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FOXE3 mutations: genotype-phenotype correlations.
Plaisancié, J; Ragge, N K; Dollfus, H; Kaplan, J; Lehalle, D; Francannet, C; Morin, G; Colineaux, H; Calvas, P; Chassaing, N.
Affiliation
  • Plaisancié J; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.
  • Ragge NK; INSERM U1056, Université Toulouse III, Toulouse, France.
  • Dollfus H; Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.
  • Kaplan J; West Midlands Regional Genetics Service, Birmingham Women and Children's NHS Foundation Trust, Birmingham, UK.
  • Lehalle D; Centre de Référence pour les affections rares en génétique ophtalmologique, CARGO, Filière SENSGENE, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
  • Francannet C; INSERM U1163, Génétique Ophtalmologique, Paris, France.
  • Morin G; Centre de Génétique et Centre de Référence "Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, Dijon, France.
  • Colineaux H; Service de Génétique Médicale, CHU Estaing, Clermont-Ferrand, France.
  • Calvas P; Service de génétique, Hôpital nord d'Amiens, Amiens, France.
  • Chassaing N; Department of Epidemiology, Health Economics and Public Health, Toulouse University Hospital, France.
Clin Genet ; 93(4): 837-845, 2018 04.
Article in En | MEDLINE | ID: mdl-29136273
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aphakia / Microphthalmos / Genetic Predisposition to Disease / Forkhead Transcription Factors Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Clin Genet Year: 2018 Type: Article Affiliation country: France
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aphakia / Microphthalmos / Genetic Predisposition to Disease / Forkhead Transcription Factors Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Clin Genet Year: 2018 Type: Article Affiliation country: France