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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Detalles Bibliográficos
Autores principales: Al-Shehhi, Halima, Gabr, Ahlam, Al-Haddabi, Intisar, Tena, Raquel, Baquero, Anna, Al-Maamari, Watfa, Al-Maawali, Almundher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: OMJ 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745418/
https://www.ncbi.nlm.nih.gov/pubmed/31555424
http://dx.doi.org/10.5001/omj.2019.83

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745418/
https://www.ncbi.nlm.nih.gov/pubmed/31555424
http://dx.doi.org/10.5001/omj.2019.83

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