All individuals with variants in gene NKX2-1

3 entries on 1 page. Showing entries 1 - 3.
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00050611 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, delayed speech and language development, macrocephaly, focal seizures with impairment of consciousness or awareness, infantile muscular hypotonia, specific learning disability, patent foramen ovale, absence seizures, downslanted palpebral fissures, narrow forehead, depressed nasal bridge, smooth philtrum, full cheeks, 2-3 toe syndactyly 1 1 Johan den Dunnen
00291033 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00374419 S-3171 PubMed: Ganapathy 2019 - - - India - - - - - ? Complex movement disorder involving motor delay, hypotonia, ataxia, myoclonus and choreoathetosis 1 1 Johan den Dunnen
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