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Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project.
Downie, Lilian; Halliday, Jane; Lewis, Sharon; Lunke, Sebastian; Lynch, Elly; Martyn, Melissa; Gaff, Clara; Jarmolowicz, Anna; Amor, David J.
  • Downie L; Victorian Clinical Genetics Services, Melbourne, Australia.
  • Halliday J; Murdoch Children's Research Institute, Melbourne, Australia.
  • Lewis S; Royal Children's Hospital, Melbourne, Australia.
  • Lunke S; Department of Paediatrics, University of Melbourne, Melbourne, Australia.
  • Lynch E; Murdoch Children's Research Institute, Melbourne, Australia.
  • Martyn M; Department of Paediatrics, University of Melbourne, Melbourne, Australia.
  • Gaff C; Murdoch Children's Research Institute, Melbourne, Australia.
  • Jarmolowicz A; Department of Paediatrics, University of Melbourne, Melbourne, Australia.
  • Amor DJ; Victorian Clinical Genetics Services, Melbourne, Australia.
Genet Med ; 22(5): 937-944, 2020 05.
Article en En | MEDLINE | ID: mdl-31974413
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tamizaje Neonatal / Sordera Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Child / Humans / Infant / Newborn Idioma: En Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tamizaje Neonatal / Sordera Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Child / Humans / Infant / Newborn Idioma: En Año: 2020 Tipo del documento: Article