All individuals with variants in gene FGG

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

ID_report     

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VIP     

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Owner     
00000028 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000085 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00017892 - PubMed: Yoshida 1988 2-generation family, affected father and 2 daugthers - - Japan - - - - - afibrinogenemia, congenital hypofibrinogenemiano history of thrombosis or hemorrhage 1 3 Johan den Dunnen
00017893 - PubMed: Terukina 1988 2-generation family, affected father and daugther - yes Japan - - - - - afibrinogenemia, congenital see paper; dysfibrinogenemia, abnormally prolonged thrombin time 1 2 Johan den Dunnen
00017894 - PubMed: Schmelzer 1989 2-generation family, affected father and daugther M ? United States - - - - - afibrinogenemia, congenital see paper 1 2 Johan den Dunnen
00143186 - - - M yes (India) Asian - - - - ? microcephaly (HP:0000252), cortical atrophy (HP:?), hypofibrinogenemia (HP:0011900) 1 1 -
00143188 - - - M yes (India) Asian - - - - ? microcephaly (HP:0000252), cortical atrophy (HP:?), hypofibrinogenemia (HP:0011900) 1 1 Joshi Stephen
00293567 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00362007 Pat10AB PubMed: Duvvari 2016 patient - - Netherlands white - - - - retinal disease - 1 1 LOVD
00438619 HSC0092 PubMed: Hamdan 2017 WGS analysis 197 individuals with unexplained DEE (unaffected parents) - - Canada - - - - pharmaco-resistant seizures DEE - 1 1 Johan den Dunnen
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