Presentation Information
[P1-08-05]A case of intellectual disability male with Xq28 microduplication telomeric to MECP2 inherited from the carrier mother
Shinsuke Ninomiya1, Yoshiyuki Hanaoka2, Takahiro Hayashi2, Toshiyuki Yamamoto3 (1. Department of Clinical Genetics, Kurashiki Central Hospital, Okayama, Japan, 2. Department of Pediatrics, Kurashiki Central Hospital, Okayama, Japan, 3. Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan)
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