All individuals with variants in gene NRXN1

5 entries on 1 page. Showing entries 1 - 5.
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00050717 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected parents F - United Kingdom (Great Britain) - - - Decipher - ? low-set ears, epicanthus, micrognathia, 2-3 toe syndactyly, muscular hypotonia, thin lips, almond-shaped palpebral fissure, global developmental delay 1 2 Johan den Dunnen
00292792 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 6 Mohammed Faruq
00292793 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 6 Mohammed Faruq
00327547 family PubMed: Beck 2014 2-generation family, 5 affected (2F, 3M) F;M yes Iraq - - - - - retinal disease see paper; ..., Leber congenital amaurosis , Joubert syndrome, polycystic kidney disease 1 5 Johan den Dunnen
00374558 S-6113 PubMed: Ganapathy 2019 - - - India - - - - - ? autistic behaviour and epilepsy 1 1 Johan den Dunnen
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