All individuals with variants in gene FGG

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

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Owner     
00000028 - PubMed: Bell 2011 - - - - - - 0 - - - - 1 1 LOVD-team, but with Curator vacancy
00000085 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 LOVD-team, but with Curator vacancy
00017892 - PubMed: Yoshida 1988 2-generation family, affected father and 2 daugthers - - Japan - - 0 - - 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 - - 0 - - 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 - - 0 - - afibrinogenemia, congenital see paper 1 2 Johan den Dunnen
00143186 - - - M yes (India) Asian - 0 - - ? microcephaly (HP:0000252), cortical atrophy (HP:?), hypofibrinogenemia (HP:0011900) 1 1 -
00143188 - - - M yes (India) Asian - 0 - - ? microcephaly (HP:0000252), cortical atrophy (HP:?), hypofibrinogenemia (HP:0011900) 1 1 Joshi Stephen
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