مرور Volume 44, Issue 4 بر اساس موضوع "DNA copy number variations"
در حال نمایش موارد 1 - 1 از 1
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Microduplication of Xp22.31 and MECP2 Pathogenic Variant in a Girl with Rett Syndrome: A Case Report
(Shiraz University of Medical Sciences, 2019-07-01)Rett syndrome (RS) is a neurodevelopmental infantile disease characterized by an early normal psychomotor development followed by a regression in the acquisition of normal developmental stages. In the majority of cases, ...



