SIX5 - branchio-oto-renal dysplasia

This test is available for the following conditions:

  • Conditions > Hearing impairment > BOR syndrome (Branchio-Oto-Renal dysplasia)
  • Conditions > Renal / Nephrological > BOR syndrome (Branchio-Oto-Renal dysplasia)

This product is also part of the following panels:

  • WES hearing impairment (97.3% **)
  • WES Mendelian inherited disorders (97.3% **)
  • WES renal disorders (97.3% **)

** % 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: 600963
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 360

Gene

EYA1 - branchio-oto-renal dysplasia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 715

EYA1 - branchio-oto-renal dysplasia



€ 715

EYA1 - branchio-oto-renal dysplasia

This test is available for the following conditions:

  • Conditions > Hearing impairment > BOR syndrome (Branchio-Oto-Renal dysplasia)
  • Conditions > Renal / Nephrological > BOR syndrome (Branchio-Oto-Renal dysplasia)

This product is also part of the following panels:

  • WES craniofacial anomalies (99.8% **)
  • WES hearing impairment (99.8% **)
  • WES Mendelian inherited disorders (99.8% **)
  • WES renal disorders (99.8% **)
  • WES vision disorders (99.8% **)

** % 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)

OMIM: 601653
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 715
Gene

SIX1 - branchio-oto-renal dysplasia

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

SIX1 - branchio-oto-renal dysplasia



€ 336

SIX1 - branchio-oto-renal dysplasia

This test is available for the following conditions:

  • Conditions > Hearing impairment > BOR syndrome (Branchio-Oto-Renal dysplasia)
  • Conditions > Renal / Nephrological > BOR syndrome (Branchio-Oto-Renal dysplasia)

This product is also part of the following panels:

  • WES craniofacial anomalies (98.7% **)
  • WES hearing impairment (98.7% **)
  • WES Mendelian inherited disorders (98.7% **)

** % 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: 601205
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 336
Gene

SIX5 - branchio-oto-renal dysplasia

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

SIX5 - branchio-oto-renal dysplasia



€ 360