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Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndrome.
Wafa, Talah T; Faridi, Rabia; King, Kelly A; Zalewski, Christopher; Yousaf, Rizwan; Schultz, Julie M; Morell, Robert J; Muskett, Julie; Turriff, Amy; Tsilou, Ekaterini; Griffith, Andrew J; Friedman, Thomas B; Zein, Wadih M; Brewer, Carmen C.
Afiliação
  • Wafa TT; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Faridi R; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • King KA; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Zalewski C; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Yousaf R; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Schultz JM; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Morell RJ; Review Analysis Department, GeneDx, Gaithersburg, Maryland, USA.
  • Muskett J; Genomics and Computational Biology Core, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Turriff A; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Tsilou E; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Griffith AJ; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Friedman TB; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Zein WM; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Brewer CC; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.
Clin Genet ; 99(2): 226-235, 2021 02.
Article em En | MEDLINE | ID: mdl-33089500
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vestíbulo do Labirinto / Síndromes de Usher Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Middle aged Idioma: En Revista: Clin Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vestíbulo do Labirinto / Síndromes de Usher Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Middle aged Idioma: En Revista: Clin Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos