DFNB59 - autosomal recessive deafness type 59

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 610219
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 369

Gene

CABP2 - autosomal recessive deafness type 93

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 360

CABP2 - autosomal recessive deafness type 93



€ 360

CABP2 - autosomal recessive deafness type 93

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 607314
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 360
Gene

CDH23 - autosomal recessive deafness type 12 (DFNB12)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 806

CDH23 - autosomal recessive deafness type 12 (DFNB12)



€ 806

CDH23 - autosomal recessive deafness type 12 (DFNB12)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES hereditary cancer (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)
  • WES vision disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 605516
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 806
Gene

CLDN14 - autosomal recessive deafness type 29 (DFNB29)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 344

CLDN14 - autosomal recessive deafness type 29 (DFNB29)



€ 344

CLDN14 - autosomal recessive deafness type 29 (DFNB29)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 605608
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 344
Gene

CLIC5 - Deafness, autosomal recessive (DFNB103)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 369

CLIC5 - Deafness, autosomal recessive (DFNB103)



€ 369

CLIC5 - Deafness, autosomal recessive (DFNB103)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 607293
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 369
Gene

DFNB59 - autosomal recessive deafness type 59

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 369

DFNB59 - autosomal recessive deafness type 59



€ 369
Gene

ESRRB - autosomal recessive deafness type 35 (DFNB35)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 402

ESRRB - autosomal recessive deafness type 35 (DFNB35)



€ 402

ESRRB - autosomal recessive deafness type 35 (DFNB35)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 608565
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 402
Gene

FGF23 - familial hyperphosphatemic tumoral calcinosis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 336

FGF23 - familial hyperphosphatemic tumoral calcinosis



€ 336

FGF23 - familial hyperphosphatemic tumoral calcinosis

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES Mendelian inherited disorders (100.0% *)
  • WES renal disorders (100.0% *)
  • WES short stature/skeletal dysplasia (100.0% *)
  • WES skin disorders¹ (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 605380
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 336
Gene

GIPC3 - autosomal recessive deafness type 15 (DFNB15)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 360

GIPC3 - autosomal recessive deafness type 15 (DFNB15)



€ 360

GIPC3 - autosomal recessive deafness type 15 (DFNB15)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 608792
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 360
Gene

GJB2/GJB6 - autosomal recessive deafness type 1 (DFNB1)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 344

GJB2/GJB6 - autosomal recessive deafness type 1 (DFNB1)



€ 344

GJB2/GJB6 - autosomal recessive deafness type 1 (DFNB1)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • PCR Deletion
Remarks
A deletion in GJB6 is also described in DFNB1. Therefore, GJB6 deletion analysis is also performed

OMIM: 121011
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 344
Gene

GRXCR1 - autosomal recessive deafness type 25 (DFNB25)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 344

GRXCR1 - autosomal recessive deafness type 25 (DFNB25)



€ 344

GRXCR1 - autosomal recessive deafness type 25 (DFNB25)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (99.3% *)
  • WES Mendelian inherited disorders (99.3% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 613283
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 344
Gene

HGF - autosomal recessive deafness type 39 (DFNB39)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 459

HGF - autosomal recessive deafness type 39 (DFNB39)



€ 459

HGF - autosomal recessive deafness type 39 (DFNB39)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 142409
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 459
Gene

ILDR1 - autosomal recessive deafness type 42 (DFNB42)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 385

ILDR1 - autosomal recessive deafness type 42 (DFNB42)



€ 385

ILDR1 - autosomal recessive deafness type 42 (DFNB42)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 609739
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 385
Gene

KARS - autosomal recessive deafness type 89

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 435

KARS - autosomal recessive deafness type 89



€ 435

KARS - autosomal recessive deafness type 89

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 601421
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 435
Gene

LOXHD1 - autosomal recessive deafness type 77 (DFNB77 )

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 657

LOXHD1 - autosomal recessive deafness type 77 (DFNB77 )



€ 657

LOXHD1 - autosomal recessive deafness type 77 (DFNB77 )

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 613072
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 657
Gene

MYO15A - autosomal recessive deafness type 3 (DFNB3)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 773

MYO15A - autosomal recessive deafness type 3 (DFNB3)



€ 773

MYO15A - autosomal recessive deafness type 3 (DFNB3)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 602666
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 773
Gene

MYO3A - autosomal recessive deafness 30 (DFNB30)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 558

MYO3A - autosomal recessive deafness 30 (DFNB30)



€ 558

MYO3A - autosomal recessive deafness 30 (DFNB30)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 606808
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 558
Gene

MYO6 - autosomal recessive deafness type 37 (DFNB37)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 600

MYO6 - autosomal recessive deafness type 37 (DFNB37)



€ 600

MYO6 - autosomal recessive deafness type 37 (DFNB37)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES heart disorders¹ (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 607821
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 600
Gene

MYO7A - autosomal recessive deafness type 2 (DFNB2)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 707

MYO7A - autosomal recessive deafness type 2 (DFNB2)



€ 707

MYO7A - autosomal recessive deafness type 2 (DFNB2)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)
  • WES vision disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 276903
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 707
Gene

OTOF - autosomal recessive deafness type 9 (DFNB9)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 699

OTOF - autosomal recessive deafness type 9 (DFNB9)



€ 699

OTOF - autosomal recessive deafness type 9 (DFNB9)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 603681
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 699
Gene

OTOG - autosomal recessive deafness type 18B (DFNB18B)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 682

OTOG - autosomal recessive deafness type 18B (DFNB18B)



€ 682

OTOG - autosomal recessive deafness type 18B (DFNB18B)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 604487
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 682
Gene

OTOGL - autosomal recessive deafness type 84B (DFNB84B)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 765

OTOGL - autosomal recessive deafness type 84B (DFNB84B)



€ 765

OTOGL - autosomal recessive deafness type 84B (DFNB84B)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 614925
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 765
Gene

PCDH15 - autosomal recessive deafness type 23 (DFNB23)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 583

PCDH15 - autosomal recessive deafness type 23 (DFNB23)



€ 583

PCDH15 - autosomal recessive deafness type 23 (DFNB23)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)
  • WES vision disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 605514
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 583
Gene

PTPRQ - autosomal recessive deafness type 84 (DFNB84)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 794

PTPRQ - autosomal recessive deafness type 84 (DFNB84)



€ 794

PTPRQ - autosomal recessive deafness type 84 (DFNB84)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (91.9% *)
  • WES Mendelian inherited disorders (91.9% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 603317
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 794
Gene

RDX - autosomal recessive deafness type 24

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 426

RDX - autosomal recessive deafness type 24



€ 426

RDX - autosomal recessive deafness type 24

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 179410
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 426
Gene

SLC26A4 - autosomal recessive deafness type 4

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 484

SLC26A4 - autosomal recessive deafness type 4



€ 484

SLC26A4 - autosomal recessive deafness type 4

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)
Remarks
MLPA analysis if only one variant has been found in an autosomal recessive disease.

OMIM: 605646
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 484
Gene

SLC26A5 - autosomal recessive deafness type 61

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 476

SLC26A5 - autosomal recessive deafness type 61



€ 476

SLC26A5 - autosomal recessive deafness type 61

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 604943
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 476
Gene

TECTA - autosomal recessive deafness type 21 (DFNB21)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 542

TECTA - autosomal recessive deafness type 21 (DFNB21)



€ 542

TECTA - autosomal recessive deafness type 21 (DFNB21)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 602574
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 542
Gene

TMC1 - autosomal recessive deafness type 7/11 (DFNB7)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 492

TMC1 - autosomal recessive deafness type 7/11 (DFNB7)



€ 492

TMC1 - autosomal recessive deafness type 7/11 (DFNB7)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 606706
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 492
Gene

TMPRSS3 - autosomal recessive deafness type 8/10 (DFNB8)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 418

TMPRSS3 - autosomal recessive deafness type 8/10 (DFNB8)



€ 418

TMPRSS3 - autosomal recessive deafness type 8/10 (DFNB8)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 605511
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 418
Gene

TPRN - autosomal recessive deafness type 79 (DFNB79)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 377

TPRN - autosomal recessive deafness type 79 (DFNB79)



€ 377

TPRN - autosomal recessive deafness type 79 (DFNB79)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (95.4% *)
  • WES Mendelian inherited disorders (95.4% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 613354
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 377
Gene

TRIOBP - autosomal recessive deafness type 28 (DFNB28)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 509

TRIOBP - autosomal recessive deafness type 28 (DFNB28)



€ 509

TRIOBP - autosomal recessive deafness type 28 (DFNB28)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 609761
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 509
Gene

USH1C (HARMONIN) - autosomal recessive deafness type 18A (DFNB18A)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 533

USH1C (HARMONIN) - autosomal recessive deafness type 18A (DFNB18A)



€ 533

USH1C (HARMONIN) - autosomal recessive deafness type 18A (DFNB18A)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal recessive

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (100.0% *)
  • WES Mendelian inherited disorders (100.0% *)
  • WES vision disorders (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 605242
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 533