Association of Congenital Cardiovascular Malformation and Neuropsychiatric Phenotypes with 15q11.2 (BP1–BP2) Deletion in the UK Biobank
European Journal of Human Genetics（2020）
关键词
Chromosome abnormality,Genetics research,Genome informatics,High-throughput screening,Neurodevelopmental disorders,Biomedicine,general,Human Genetics,Bioinformatics,Gene Expression,Cytogenetics
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