首页>American journal of medical genetics, Part A>Compound heterozygous microdeletion of chromosome 15q13.3 region in a child with hypotonia, impaired vision, and global developmental delay
Compound heterozygous microdeletion of chromosome 15q13.3 region in a child with hypotonia, impaired vision, and global developmental delay
作者单位：Detroit Medical Center University Laboratories, Cytogenetics Laboratory, Detroit, MI, United States[1]Division of Genetics and Metabolic Disorders, Department of Pediatrics, Wayne State University[2]Division of Pediatric Neurology, Department of Pediatrics, Wayne State University School of[3]
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