New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
第一作者:
Gerarda,Cappuccio
第一单位:
Department of Translational Medical Sciences, Section of Pediatrics, Federico II University, Via Sergio Pansini 5, 80131, Naples, Italy.
作者:
主题词
畸形, 多发性(Abnormalities, Multiple);青少年(Adolescent);儿童(Child);儿童, 学龄前(Child, Preschool);染色体畸变(Chromosome Aberrations);比较基因组杂交(Comparative Genomic Hybridization);DNA拷贝数变异(DNA Copy Number Variations);女(雌)性(Female);人类(Humans);婴儿(Infant);男(雄)性(Male);青年人(Young Adult)
DOI
10.1186/s13052-016-0246-7
PMID
27072107
发布时间
2022-03-31
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