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Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate.
Breckpot, Jeroen; Anderlid, Britt-Marie; Alanay, Yasemin; Blyth, Moira; Brahimi, Afane; Duban-Bedu, Bénédicte; Gozé, Odile; Firth, Helen; Yakicier, Mustafa Cengiz; Hens, Greet; Rayyan, Maissa; Legius, Eric; Vermeesch, Joris Robert; Devriendt, Koen.
Afiliação
  • Breckpot J; Center for Human Genetics, University Hospitals Leuven and Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Anderlid BM; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
  • Alanay Y; Pediatric Genetics Unit, Department of Pediatrics, Acibadem University School of Medicine, Istanbul, Turkey.
  • Blyth M; Yorkshire Regional Genetics Service, Chapel Allerton Hospital, Leeds, UK.
  • Brahimi A; Centre de Génétique Chromosomique, Hôpital St-Vincent-de-Paul, GHICL, Lille, France.
  • Duban-Bedu B; Centre de Génétique Chromosomique, Hôpital St-Vincent-de-Paul, GHICL, Lille, France.
  • Gozé O; Service Pédiatrie, Centre Hospitalier de Valenciennes, Valenciennes, France.
  • Firth H; Department of Clinical Genetics, East Anglian Medical Genetics Service, Addenbrooke's Hospital, Cambridge, UK.
  • Yakicier MC; Department of Molecular Biology and Genetics, Acibadem University, Istanbul, Turkey.
  • Hens G; ENT Department, University Hospitals Leuven, Leuven, Belgium.
  • Rayyan M; Neonatology Unit, University Hospitals Leuven, Leuven, Belgium.
  • Legius E; Center for Human Genetics, University Hospitals Leuven and Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Vermeesch JR; Center for Human Genetics, University Hospitals Leuven and Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Devriendt K; Center for Human Genetics, University Hospitals Leuven and Department of Human Genetics, KU Leuven, Leuven, Belgium.
Eur J Hum Genet ; 24(1): 51-8, 2016 Jan.
Article em En | MEDLINE | ID: mdl-25944382
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 22 / Neuroma Acústico / Deleção Cromossômica / Fissura Palatina / Proteínas Supressoras de Tumor / Agenesia do Corpo Caloso Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Animals / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 22 / Neuroma Acústico / Deleção Cromossômica / Fissura Palatina / Proteínas Supressoras de Tumor / Agenesia do Corpo Caloso Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Animals / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article