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

BACKGROUND: 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 perinatal features of 134 Chinese individuals with PWS. METHODS: This study inclu...

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Detalles Bibliográficos
Autores principales: Yang, Lili, Zhou, Qiong, Ma, Bo, Mao, Shujiong, Dai, Yanli, Zhu, Mingqiang, Zou, Chaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975078/
https://www.ncbi.nlm.nih.gov/pubmed/31964399
http://dx.doi.org/10.1186/s13023-020-1306-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975078/
https://www.ncbi.nlm.nih.gov/pubmed/31964399
http://dx.doi.org/10.1186/s13023-020-1306-z

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