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Research article Open access

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

Halima Al-Shehhi, Ahlam Gabr, Intisar Al-Haddabi et al. · Oman Medical Journal · 2019 · 10.5001/omj.2019.83

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 syndrome was reported to …

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