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  1. Article

    Open Access

    Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region

    Prader-Willi syndrome (PWS) is a neurobehavioral disorder characterized by neonatal hypotonia, childhood obesity, dysmorphic features, hypogonadism, mental retardation, and behavioral problems. Although PWS is...

    Yong-hui Jiang, Kekio Wauki, Qian Liu, Jan Bressler, Yanzhen Pan in BMC Genomics (2008)