المؤلفون: Lance W. Patterson, Xueqing Wang, Fatima Boricha, Sophia Ali, Seema R. Lalani, Carlos A. Bacino, Brian Dawson, James R. Lupski, Chumei Li, Chad A. Shaw, Patricia Hixson, John L. Jefferies, Runako Whittaker, Aamir Malik, Ankita Patel, Pawel Stankiewicz, Katarzyna E. Kolodziejska, Przemyslaw Szafranski, Zhishuo Ou, Stephanie M. Ware, Sung Hae L. Kang, Arthur L. Beaudet, Qi Tian, John W. Belmont, Lorraine Potocki, Daniel J. Penny, Amina Jinnah, Sau Wai Cheung

المصدر: European journal of human genetics : EJHG. 21(2)

مصطلحات موضوعية: Male, DNA Copy Number Variations, Chromosomes, Human, Pair 22, Chromosome Disorders, Biology, Bioinformatics, Polymorphism, Single Nucleotide, Article, Cohort Studies, Genetics, Humans, In patient, Genetic Predisposition to Disease, Copy-number variation, Eye Abnormalities, Protein Interaction Maps, Gene, Genetics (clinical), Sequence Deletion, Aneuploidy, DNA Copy Number Variants, Cardiovascular Diseases, Cohort, Cardiovascular malformations, Female, Chromosomes, Human, Pair 16, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffedf6daaa3da83a36de3bdad618a80a
https://pubmed.ncbi.nlm.nih.gov/22929023