DVL1 - Robinow syndrome
This test is available for the following conditions:
- Conditions > Multiple congenital anomalies (MCA) > Robinow syndrome
- Conditions > Skeletal > Robinow syndrome
This product is also part of the following panels:
- Mendelian inherited disorders panel with genome wide CNV analysis
- Orofacial clefting panel with genome wide CNV analysis
- Short stature/skeletal dysplasia panel with genome wide CNV analysis
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of selected exons and flanking intron-exon boundaries
Only exon 14 of the DVL1 gene will be tested, since all reported (activating) mutations are located in the penultimate exon (exon 14) of the DVL1 gene (White et al., Am J Hum Genet. 2015 Apr 2;96(4):612-22).
OMIM:
601365
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
DVL3 - Robinow syndrome
This test is available for the following conditions:
- Conditions > Multiple congenital anomalies (MCA) > Robinow syndrome
- Conditions > Skeletal > Robinow syndrome
This product is also part of the following panels:
- Congenital heartdisease panel¹
- Heart disorders panel¹
- Mendelian inherited disorders panel with genome wide CNV analysis
- Orofacial clefting panel with genome wide CNV analysis
- Short stature/skeletal dysplasia panel with genome wide CNV analysis
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of selected exons and flanking intron-exon boundaries
OMIM:
601368
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
WNT5A - Robinow syndrome
This test is available for the following conditions:
- Conditions > Multiple congenital anomalies (MCA) > Robinow syndrome
- Conditions > Skeletal > Robinow syndrome
This product is also part of the following panels:
- Mendelian inherited disorders panel with genome wide CNV analysis
- Orofacial clefting panel with genome wide CNV analysis
- Short stature/skeletal dysplasia panel with genome wide CNV analysis
- Skin disorders panel¹
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
180700
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane