Your browser doesn't support javascript.
loading
A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.
Jacquemont, Sébastien; Coe, Bradley P; Hersch, Micha; Duyzend, Michael H; Krumm, Niklas; Bergmann, Sven; Beckmann, Jacques S; Rosenfeld, Jill A; Eichler, Evan E.
Afiliación
  • Jacquemont S; Service of Medical Genetics, University Hospital of Lausanne, University of Lausanne, Lausanne 1011, Switzerland. Electronic address: sebastien.jacquemont@chuv.ch.
  • Coe BP; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Hersch M; Department of Medical Genetics, University of Lausanne, Lausanne 1005, Switzerland; Swiss institute of Bioinformatics, Lausanne 1015, Switzerland.
  • Duyzend MH; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Krumm N; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
  • Bergmann S; Department of Medical Genetics, University of Lausanne, Lausanne 1005, Switzerland; Swiss institute of Bioinformatics, Lausanne 1015, Switzerland.
  • Beckmann JS; Swiss institute of Bioinformatics, Lausanne 1015, Switzerland.
  • Rosenfeld JA; Signature Genomic Laboratories LLC, PerkinElmer Inc., Spokane, WA 99207, USA.
  • Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA; Howard Hughes Medical Institute. Electronic address: eee@gs.washington.edu.
Am J Hum Genet ; 94(3): 415-25, 2014 Mar 06.
Article en En | MEDLINE | ID: mdl-24581740
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Discapacidades del Desarrollo / Trastornos Generalizados del Desarrollo Infantil / Mutación Tipo de estudio: Etiology_studies / Health_economic_evaluation / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Hum Genet Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Discapacidades del Desarrollo / Trastornos Generalizados del Desarrollo Infantil / Mutación Tipo de estudio: Etiology_studies / Health_economic_evaluation / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Hum Genet Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos