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Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype.
Doddato, Gabriella; Fabbiani, Alessandra; Fallerini, Chiara; Bruttini, Mirella; Hadjistilianou, Theodora; Landi, Martino; Coradeschi, Caterina; Grosso, Salvatore; Tomasini, Barbara; Mencarelli, Maria Antonietta; Renieri, Alessandra; Ariani, Francesca.
Afiliação
  • Doddato G; Medical Genetics, University of Siena, Siena, Tuscany, Italy.
  • Fabbiani A; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Tuscany, Italy.
  • Fallerini C; Medical Genetics, University of Siena, Siena, Tuscany, Italy.
  • Bruttini M; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Tuscany, Italy.
  • Hadjistilianou T; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy.
  • Landi M; Medical Genetics, University of Siena, Siena, Tuscany, Italy.
  • Coradeschi C; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Tuscany, Italy.
  • Grosso S; Medical Genetics, University of Siena, Siena, Tuscany, Italy.
  • Tomasini B; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Tuscany, Italy.
  • Mencarelli MA; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy.
  • Renieri A; Ophthalmological Science and Neuroscience, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy.
  • Ariani F; Terapia Intensiva Neonatale, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy.
Front Genet ; 14: 1143795, 2023.
Article em En | MEDLINE | ID: mdl-36761000
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article