Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders.
第一作者:
Marta,Arpone
第一单位:
Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia; Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia; Brain and Mind, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia.
作者:
主题词
儿童(Child);男(雄)性(Male);女(雌)性(Female);人类(Humans);脆性X综合征(Fragile X Syndrome);Prader-Willi综合征(Prader-Willi Syndrome);染色体, 人, 15对(Chromosomes, Human, Pair 15);双亲(Parents)
DOI
10.1016/j.ridd.2022.104338
PMID
36179574
发布时间
2022-11-29
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