Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation.
第一作者:
Gregory Ryan,Handrigan
第一单位:
Division of Nephrology, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, Canada M5G1X8. norman.rosenblum@sickkids.ca
作者:
医学主题词
青少年(Adolescent);儿童(Child);儿童发育障碍, 广泛性(Child Development Disorders, Pervasive);儿童, 学龄前(Child, Preschool);染色体图(Chromosome Mapping);染色体, 人, 16对(Chromosomes, Human, Pair 16);DNA拷贝数变异(DNA Copy Number Variations);女(雌)性(Female);基因缺失(Gene Deletion);人类(Humans);婴儿(Infant);婴儿, 新生(Infant, Newborn);肾(Kidney);男(雄)性(Male);阻遏蛋白质类(Repressor Proteins);青年人(Young Adult)
DOI
10.1136/jmedgenet-2012-101288
PMID
23335808
发布时间
2013-02-14
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