All individuals with variants in gene PPEF2

10 entries on 1 page. Showing entries 1 - 10.
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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     

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Panel size     

Owner     
00050201 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050303 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050308 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050321 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050334 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050335 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00231413 Fam22 PubMed: Cox 2019 3-generation family, 3 affected (2F, M) F;M - Colombia - - - - - CLP - 1 3 Timothy Cox
00407356 RP-95 PubMed: Borràs 2013 - - - Spain Spanish - - - - retinal disease - 1 1 LOVD
00407357 RP-645 PubMed: Borràs 2013 - - - Spain Spanish - - - - retinal disease - 1 1 LOVD
00407358 RP-83 PubMed: Borràs 2013 - - - Spain Spanish - - - - retinal disease - 2 1 LOVD
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