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Novel Variants of SOX4 in Patients with Intellectual Disability.
Grosse, Martin; Kuechler, Alma; Dabir, Tabib; Spranger, Stephanie; Beck-Wödl, Stefanie; Bertrand, Miriam; Haack, Tobias B; Grasemann, Corinna; Manka, Eva; Depienne, Christel; Kaiser, Frank J.
Afiliação
  • Grosse M; Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, 47057 Duisburg, Germany.
  • Kuechler A; Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, 47057 Duisburg, Germany.
  • Dabir T; Northern Ireland Regional Genetics Service, Belfast City Hospital, Belfast BT9 7AB, UK.
  • Spranger S; Limbach Genetics, 28209 Bremen, Germany.
  • Beck-Wödl S; Medical Genetics and Applied Genomics, University of Tuebingen, 72076 Tuebingen, Germany.
  • Bertrand M; Medical Genetics and Applied Genomics, University of Tuebingen, 72076 Tuebingen, Germany.
  • Haack TB; Medical Genetics and Applied Genomics, University of Tuebingen, 72076 Tuebingen, Germany.
  • Grasemann C; Department of Pediatrics, Faculty of Medicine, Ruhr University of Bochum, 44791 Bochum, Germany.
  • Manka E; Center for Rare Disease Essen (Essener Zentrum für Seltene Erkrankungen-EZSE), Universitätsmedizin Essen, 45147 Essen, Germany.
  • Depienne C; Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, 47057 Duisburg, Germany.
  • Kaiser FJ; Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, 47057 Duisburg, Germany.
Int J Mol Sci ; 24(4)2023 Feb 09.
Article em En | MEDLINE | ID: mdl-36834931
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Fatores de Transcrição SOXC / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Fatores de Transcrição SOXC / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha