Výsledky vyhledávání - "Madiha Mohamed"

Akademický článek

Identification of a novel CTCF mutation responsible for syndromic intellectual disability – a case report

Autor: Fatma Bastaki, Pratibha Nair, Madiha Mohamed, Ethar Mustafa Malik, Mustafa Helmi, Mahmoud Taleb Al-Ali, Abdul Rezzak Hamzeh

Publikováno v: BMC Medical Genetics, Vol 18, Iss 1, Pp 1-6 (2017)

Abstract Background Autosomal dominant mental retardation 21 (MRD21) is a very rare condition, characterized by short stature, microcephaly, mild facial dysmorphisms and intellectual disability that ranged from mild to severe. MRD21 is caused by muta

Externí odkaz: https://doaj.org/article/e9f9b479dd284f109db6422496b298c8

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