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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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| Publicat a: | Oman Med J |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
OMJ
2019
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| Matèries: | |
| Accés en línia: | 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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