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Correction: Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia.
Kesim, Yesim; Ceroni, Fabiola; Damián, Alejandra; Blanco-Kelly, Fiona; Ayuso, Carmen; Williamson, Kathy; Paquis-Flucklinger, Véronique; Bax, Dorine A; Plaisancié, Julie; Rieubland, Claudine; Chamlal, Mostafa; Cortón, Marta; Chassaing, Nicolas; Calvas, Patrick; Ragge, Nicola K.
Afiliación
  • Kesim Y; Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.
  • Ceroni F; Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.
  • Damián A; Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
  • Blanco-Kelly F; Department of Genetics & Genomics, Instituto de Investigación Sanitaria-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain.
  • Ayuso C; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Madrid, Spain.
  • Williamson K; Department of Genetics & Genomics, Instituto de Investigación Sanitaria-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain.
  • Paquis-Flucklinger V; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Madrid, Spain.
  • Bax DA; Department of Genetics & Genomics, Instituto de Investigación Sanitaria-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain.
  • Plaisancié J; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Madrid, Spain.
  • Rieubland C; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Edinburgh, UK.
  • Chamlal M; Department of Medical Genetics, Nice Teaching Hospital, Nice, France.
  • Cortón M; Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.
  • Chassaing N; INSERM U1214, ToNIC, Université Toulouse III, Toulouse, France.
  • Calvas P; Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, CHU Toulouse, Toulouse, France.
  • Ragge NK; Department of Human Genetics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Eur J Hum Genet ; 31(10): 1196-1198, 2023 Oct.
Article en En | MEDLINE | ID: mdl-37106145
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article