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Atypical and ultra-rare Usher syndrome: a review.
Nolen, Rosalie M; Hufnagel, Robert B; Friedman, Thomas B; Turriff, Amy E; Brewer, Carmen C; Zalewski, Christopher K; King, Kelly A; Wafa, Talah T; Griffith, Andrew J; Brooks, Brian P; Zein, Wadih M.
Afiliación
  • Nolen RM; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA.
  • Hufnagel RB; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA.
  • Friedman TB; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA.
  • Turriff AE; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA.
  • Brewer CC; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA.
  • Zalewski CK; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA.
  • King KA; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA.
  • Wafa TT; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA.
  • Griffith AJ; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA.
  • Brooks BP; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA.
  • Zein WM; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA.
Ophthalmic Genet ; 41(5): 401-412, 2020 10.
Article en En | MEDLINE | ID: mdl-32372680
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Aberraciones Cromosómicas / Enfermedades Raras / Síndromes de Usher Tipo de estudio: Guideline Límite: Animals / Humans Idioma: En Revista: Ophthalmic Genet Asunto de la revista: GENETICA MEDICA / OFTALMOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Aberraciones Cromosómicas / Enfermedades Raras / Síndromes de Usher Tipo de estudio: Guideline Límite: Animals / Humans Idioma: En Revista: Ophthalmic Genet Asunto de la revista: GENETICA MEDICA / OFTALMOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos