Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice. [electronic resource]
- Journal of medical genetics 10 2019
- 701-710 p. digital
Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
1468-6244
10.1136/jmedgenet-2018-105879 doi
Autistic Disorder--genetics Case-Control Studies Cohort Studies DNA Copy Number Variations Epilepsy--genetics Female Heart Diseases--congenital Humans Intellectual Disability--genetics Loss of Function Mutation Male Neurodevelopmental Disorders--genetics Sequence Deletion