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Autor:
Tkemaladze Tinatin, Bregvadze Kakha, Gogoberishvili Mikheil, Sopromadze-Diebold Tamari, Abzianidze Elene
Publikováno v:
SAGE Open Medical Case Reports, Vol 11 (2023)
Chopra-Amiel-Gordon syndrome (OMIM: 619504) is an autosomal dominant neurodevelopmental disorder characterized by developmental delay, intellectual disability, speech delay, epilepsy, dysmorphic craniofacial features, ophthalmological abnormalities,
Externí odkaz:
https://doaj.org/article/a6bfe30e8c5243678f565c9c87a04e1e