中国实用儿科杂志
• 病例报告 • 上一篇
出版日期:
发布日期:
Online:
Published:
关键词: Prader-Willi综合征, 临床表型, 基因印记, 肌张力低下
Key words: Prader-Willi syndrome, clinical phenotype, genetic imprinting, hypotonia
全莹禹a,张 京b,冯小伟a. 婴幼儿Prader-Willi综合征2例报告[J]. 中国实用儿科杂志, DOI: 10.19538/j.ek2018060618.
QUAN Ying-yu,ZHANG Jing,FENG Xiao-wei. Report of two cases of Prader-Willi syndrome in infants[J]. CJPP, DOI: 10.19538/j.ek2018060618.
0 / 推荐
导出引用管理器 EndNote|Ris|BibTeX
链接本文: http://www.zgsyz.com/zgsyek/CN/10.19538/j.ek2018060618
http://www.zgsyz.com/zgsyek/CN/Y2018/V33/I6/478