All individuals with variants in gene PIBF1

7 entries on 1 page. Showing entries 1 - 7.
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AscendingIndividual ID     

ID_report     

Reference     

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Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

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Disease     

Phenotype details     

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Owner     
00248827 Fam PubMed: Hebbar 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F yes India - - - - - JBTS see paper; ..., global developmental delay 1 1 Johan den Dunnen
00248828 FamH1Pat3/P4 PubMed: Wheway 2015 2-generation family, affected brother/sister, unaffected heterozygous carrier parents/relatives F;M - United States Schmiedeleut Hutterite - - - - JBTS see paper; ... 1 2 Johan den Dunnen
00248829 FamH2P3/P4 PubMed: Wheway 2015 2-generation family, affected brother/sister, unaffected heterozygous carrier parents/relatives F;M - United States Schmiedeleut Hutterite - - - - JBTS see paper; ... 1 2 Johan den Dunnen
00248830 FamH3P3 PubMed: Wheway 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F - United States Schmiedeleut Hutterite - - - - JBTS see paper; ... 1 1 Johan den Dunnen
00248831 FamH4P3 PubMed: Wheway 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M - United States Schmiedeleut Hutterite 15d - - - JBTS see paper; ... 1 1 Johan den Dunnen
00248832 FamUW155P3 PubMed: Wheway 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F - United States Schmiedeleut Hutterite 15d - - - JBTS see paper; ..., narrow thorax, pelvic bone malformation, retinal degeneration due to cone-rod dystrophy in childhood, no impairment renal function 2 1 Johan den Dunnen
00290956 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 42 Mohammed Faruq
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