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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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| 發表在: | Oman Med J |
|---|---|
| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
OMJ
2019
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| 主題: | |
| 在線閱讀: | 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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