All individuals with variants in gene FBLN1

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

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Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00050175 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050185 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050227 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050298 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00293146 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00293147 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 47 Mohammed Faruq
00314708 - PubMed: Slavotinek 2015 - M - United States Hispanic - - - - ? bilateral anophthalmia, lateral facial cleft, syndactyly 1 1 Johan den Dunnen
00361999 Pat2AB PubMed: Duvvari 2016 patient - - Netherlands white - - - - retinal disease - 1 1 LOVD
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