Further Clinical and Molecular Delineation of Xp11.22 Deletion Syndrome: A Case Report

Intellectual disability (ID) is the most common diagnosis noted among children with genetic disorders. It causes social and economic burden to families and communities. The genetic causes are not completely understood, and there is significant heterogeneity. Recently, a new chromosomal X-linked synd...

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Detalhes bibliográficos
Publicado no:Oman Med J
Main Authors: Al-Shehhi, Halima, Gabr, Ahlam, Al-Haddabi, Intisar, Tena, Raquel, Baquero, Anna, Al-Maamari, Watfa, Al-Maawali, Almundher
Formato: Artigo
Idioma:Inglês
Publicado em: OMJ 2019
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6745418/
https://ncbi.nlm.nih.gov/pubmed/31555424
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5001/omj.2019.83
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