All individuals with variants in gene SCN7A

5 entries on 1 page. Showing entries 1 - 5.
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AscendingIndividual ID     

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Owner     
00050245 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00292344 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 89 Mohammed Faruq
00292345 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00304708 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00374137 - PubMed: Lefebvre 2021 fetus F - France - - - - - ? 22w-fetus, ultrasound Holoprosencephaly; autopsy intrauterine growth retardation, microcephaly, bilateral, ablepharon, corpus callosum agenesis, myelomeningocele, tracheal atresia, absent nipples, unilateral simian crease, hypoplastic phalanges, 2 1 Johan den Dunnen
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