학술논문
Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1–BP2) deletion in the UK Biobank
Document Type
Article
Author
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, 1 September 2020, 28(9):1265-1273)
Subject
Language
English
ISSN
14765438
10184813
10184813