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NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition?
Scholz, Caroline; Steinemann, Doris; Mälzer, Madeleine; Roy, Mandy; Arslan-Kirchner, Mine; Illig, Thomas; Schmidtke, Jörg; Stuhrmann, Manfred.
  • Scholz C; Institute of Human Genetics, Hannover Medical School, Hannover, Germany. Electronic address: scholz.caroline@mh-hannover.de.
  • Steinemann D; Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Mälzer M; Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Roy M; Psychiatric Clinic, Hannover Medical School, Hannover, Germany.
  • Arslan-Kirchner M; Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Illig T; Institute of Human Genetics, Hannover Medical School, Hannover, Germany; Hannover Unified Biobank, Germany.
  • Schmidtke J; Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Stuhrmann M; Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
Eur J Med Genet ; 59(10): 493-8, 2016 Oct.
Article en En | MEDLINE | ID: mdl-27596683
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Molécula L1 de Adhesión de Célula Nerviosa / Megalencefalia / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Child / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Autístico / Molécula L1 de Adhesión de Célula Nerviosa / Megalencefalia / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Child / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article