All individuals with variants in gene NEDD4L

5 entries on 1 page. Showing entries 1 - 5.
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00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 2 1 Yu Sun
00050538 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, muscular hypotonia, short philtrum, upslanted palpebral fissure 1 1 Johan den Dunnen
00276082 Case1 PubMed: Stouffs 2020 2-generation family, 1 affected, unaffected non-carrier parents M no Belgium white - - - - PVNH severe neurodevelopmental delay, seizures, hypospadias, MRI revealed bilateral periventricular nodular heterotopia and perisylvian polymicrogyria 1 1 Katrien Stouffs
00276083 FamCase2 family, 4 affected PubMed: Stouffs 2020 M no Belgium white - - - - PVNH severe neurodevelopmental delay, refractory seizures, bilateral periventricular nodular heterotopia, perisylvian polymicrogyria 1 4 Katrien Stouffs
00374787 S-1386 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
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