Increased female autosomal burden of rare copy number variants in human populations and in autism families.

Desachy, G; Croen, L A; Torres, A R; Kharrazi, M; Delorenze, G N; Windham, G C; Yoshida, C K; Weiss, L A

Desachy, G; Croen, L A; Torres, A R; Kharrazi, M; Delorenze, G N; Windham, G C; Yoshida, C K; Weiss, L A.

Affiliation

Desachy G; Department of Psychiatry and Institute for Human Genetics, UCSF, San Francisco, CA, USA.
Croen LA; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Torres AR; Center for Persons with Disabilities, Utah State University, Logan, UT, USA.
Kharrazi M; Genetic Disease Screening Program, California Department of Public Health, Richmond, CA, USA.
Delorenze GN; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Windham GC; Division of Environmental and Occupational Disease Control, California Department of Public Health, Richmond, CA, USA.
Yoshida CK; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Weiss LA; Department of Psychiatry and Institute for Human Genetics, UCSF, San Francisco, CA, USA.

Mol Psychiatry ; 20(2): 170-5, 2015 Feb.

Article de En | MEDLINE | ID: mdl-25582617

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Santé de la famille / Prédisposition génétique à une maladie / Polymorphisme de nucléotide simple / Variations de nombre de copies de segment d'ADN / Trouble du spectre autistique Type d'étude: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limites: Female / Humans / Male / Newborn / Pregnancy Langue: En Journal: Mol Psychiatry Sujet du journal: BIOLOGIA MOLECULAR / PSIQUIATRIA Année: 2015 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Royaume-Uni

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