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Genetics in Medicine, ISSN 1098-3600, 04/2019, Volume 21, Issue 4, pp. 816 - 825
Purpose: To assess the contribution of rare variants in the genetic background toward variability of neurodevelopmental phenotypes in individuals with rare... 
CNV | phenotypic variability | 16p11.2 deletion | autism | modifier | SUPPORTS | SCHIZOPHRENIA | MODEL | REARRANGEMENTS | PENETRANCE | GENETICS & HEREDITY | 16P12.1 | MUTATIONS | DELETIONS | EXPRESSION | Families & family life | Genes | Family medical history | Life Sciences | Genetics | Human genetics
Journal Article
PLoS Genetics, ISSN 1553-7390, 07/2011, Volume 7, Issue 7, p. e1002173
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Epilepsia, ISSN 0013-9580, 05/2006, Volume 47, Issue 5, pp. 830 - 838
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