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Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.

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Title: Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
Authors: Pollak RM; 1Genetics and Molecular Biology, Laney Graduate School, Emory University, Atlanta, USA., Murphy MM; 2Department of Human Genetics, School of Medicine, Emory University, Atlanta, USA., Epstein MP; 2Department of Human Genetics, School of Medicine, Emory University, Atlanta, USA., Zwick ME; 2Department of Human Genetics, School of Medicine, Emory University, Atlanta, USA.; 3Department of Pediatrics, School of Medicine, Emory University, Atlanta, USA., Klaiman C; 3Department of Pediatrics, School of Medicine, Emory University, Atlanta, USA.; 4Marcus Autism Center, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, USA., Saulnier CA; 3Department of Pediatrics, School of Medicine, Emory University, Atlanta, USA., Mulle JG; 2Department of Human Genetics, School of Medicine, Emory University, Atlanta, USA.; 5Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, USA.; Whitehead 305M, 615 Michael Street, Atlanta, GA 30322 USA.
Corporate Authors: Emory 3q29 Project
Source: Molecular autism [Mol Autism] 2019 Jul 16; Vol. 10, pp. 30. Date of Electronic Publication: 2019 Jul 16 (Print Publication: 2019).
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101534222 Publication Model: eCollection Cited Medium: Internet ISSN: 2040-2392 (Electronic) NLM ISO Abbreviation: Mol Autism Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
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              Text: 2019 Jul 16
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