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Genetics of Childhood Hearing Loss.
Mitchell, Calli Ober; Morton, Cynthia Casson.
Afiliación
  • Mitchell CO; Department of Obstetrics and Gynecology, Brigham and Women's Hospital, NRB 160, 77 Avenue Louis Pasteur, Boston, MA 02115, USA. Electronic address: https://twitter.com/CalliMitchell3.
  • Morton CC; Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Harvard Medical School, NRB 160, 77 Avenue Louis Pasteur, Boston, MA 02115, USA; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA; Broad Institute of MIT and Harvard, Cambridge, MA, USA; Manchester Centre for Audiology and Deafness, School of Health Sciences, University of Manchester, UK. Electronic address: cmorton@bwh.harvard.edu.
Otolaryngol Clin North Am ; 54(6): 1081-1092, 2021 Dec.
Article en En | MEDLINE | ID: mdl-34774226
ABSTRACT
Compelling evidence indicates that some newborns harboring genetic variants associated with hearing loss might not be identified by current physiologic newborn hearing screening (NBHS) rendering current NBHS protocols suboptimal. Incorporating genomic sequencing into NBHS would improve clinical diagnosis and decrease time to early intervention efforts.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sordera / Pérdida Auditiva Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies Límite: Humans / Newborn Idioma: En Revista: Otolaryngol Clin North Am Año: 2021 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sordera / Pérdida Auditiva Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies Límite: Humans / Newborn Idioma: En Revista: Otolaryngol Clin North Am Año: 2021 Tipo del documento: Article