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Key words: Prader-Willi syndrome, clinical phenotype, genetic imprinting, hypotonia
关键词: Prader-Willi综合征, 临床表型, 基因印记, 肌张力低下
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.
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.
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URL: http://www.zgsyz.com/zgsyek/EN/10.19538/j.ek2018060618
http://www.zgsyz.com/zgsyek/EN/Y2018/V33/I6/478