All individuals with variants in gene ORC1

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

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VIP     

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Owner     
00050659 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected and affected2nd degree relatives F - United Kingdom (Great Britain) - - - Decipher - ? feeding difficulties in infancy, seizures, poor head control, seizures, microcephaly, specific learning disability, congenital cataract, global developmental delay 1 1 Johan den Dunnen
00289873 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 20 Mohammed Faruq
00289874 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00289875 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 16 Mohammed Faruq
00289876 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 19 Mohammed Faruq
00387840 M8900109 PubMed: Hu 2019 family, 2 affected individuals - - - Lur - - - - ID syndromic intellectual disability, microcephaly, epilepsy 1 2 Johan den Dunnen
00387911 M9200021 PubMed: Hu 2019 family, 2 affected individuals, first cousin parents - yes - Turkmenistan - - - - ID syndromic intellectual disability, microcephaly 1 2 Johan den Dunnen
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