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The clinical relevance of intragenic NRXN1 deletions.
Cosemans, Nele; Vandenhove, Laura; Vogels, Annick; Devriendt, Koenraad; Van Esch, Hilde; Van Buggenhout, Griet; Olivié, Hilde; de Ravel, Thomy; Ortibus, Els; Legius, Eric; Aerssens, Peter; Breckpot, Jeroen; R Vermeesch, Joris; Shen, Sanbing; Fitzgerald, Jacqueline; Gallagher, Louise; Peeters, Hilde.
Afiliação
  • Cosemans N; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Vandenhove L; Leuven Autism Research (LAuRes), KU Leuven, Leuven, Belgium.
  • Vogels A; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Devriendt K; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Van Esch H; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Van Buggenhout G; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Olivié H; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • de Ravel T; Center for Developmental Disabilities Leuven, Leuven, Belgium.
  • Ortibus E; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Legius E; Center for Developmental Disabilities Leuven, Leuven, Belgium.
  • Aerssens P; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Breckpot J; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • R Vermeesch J; Leuven Autism Research (LAuRes), KU Leuven, Leuven, Belgium.
  • Shen S; Pediatric Department, Jessa Hospital, Hasselt, Belgium.
  • Fitzgerald J; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Gallagher L; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Peeters H; Regenerative Medicine Institute, School of Medicine, BioMedical Sciences Building, National University of Ireland (NUI), Galway, Ireland.
J Med Genet ; 57(5): 347-355, 2020 05.
Article em En | MEDLINE | ID: mdl-31932357
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Proteínas de Ligação ao Cálcio / Deleção de Genes / Moléculas de Adesão de Célula Nervosa / Deficiência Intelectual Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: J Med Genet Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Bélgica
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Proteínas de Ligação ao Cálcio / Deleção de Genes / Moléculas de Adesão de Célula Nervosa / Deficiência Intelectual Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: J Med Genet Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Bélgica