Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients | Orphanet Journal of Rare Diseases | Full Text

Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients | Orphanet Journal of Rare Diseases | Full Text

Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients

Prader-Willi syndrome (PWS) is a rare and complex genetic disorder caused by lacking expression of imprinted genes on the paternally derived chromosome 15q11-q13 region. This study aimed to characterize the pe...

Authors:Lili Yang, Qiong Zhou, Bo Ma, Shujiong Mao, Yanli Dai, Mingqiang Zhu and Chaochun Zou

Citation:Orphanet Journal of Rare Diseases 2020 15:24

Content type:Research

Published on: 21 January 2020

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