19P13.2 Microdeletion Including NFIX Associated with Overgrowth and Intellectual Disability Suggestive of Malan Syndrome
Molecular Cytogenetics（2016）
关键词
Deletion 19p13.2-13.13,Deletion 5q35.2,NSD1,SNP-array,Epigenetic diseases,Microarrays-based candidate gene strategy
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