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Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients.
Cabanillas, Rubén; Diñeiro, Marta; Cifuentes, Guadalupe A; Castillo, David; Pruneda, Patricia C; Álvarez, Rebeca; Sánchez-Durán, Noelia; Capín, Raquel; Plasencia, Ana; Viejo-Díaz, Mónica; García-González, Noelia; Hernando, Inés; Llorente, José L; Repáraz-Andrade, Alfredo; Torreira-Banzas, Cristina; Rosell, Jordi; Govea, Nancy; Gómez-Martínez, Justo Ramón; Núñez-Batalla, Faustino; Garrote, José A; Mazón-Gutiérrez, Ángel; Costales, María; Isidoro-García, María; García-Berrocal, Belén; Ordóñez, Gonzalo R; Cadiñanos, Juan.
Affiliation
  • Cabanillas R; Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA) S. A, Avda. Richard Grandío s/n, 33193, Oviedo, Spain. rcabanillas@imoma.es.
  • Diñeiro M; Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA) S. A, Avda. Richard Grandío s/n, 33193, Oviedo, Spain.
  • Cifuentes GA; Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA) S. A, Avda. Richard Grandío s/n, 33193, Oviedo, Spain.
  • Castillo D; Disease Research And Medicine (DREAMgenics) S. L., Oviedo, Spain.
  • Pruneda PC; Disease Research And Medicine (DREAMgenics) S. L., Oviedo, Spain.
  • Álvarez R; Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA) S. A, Avda. Richard Grandío s/n, 33193, Oviedo, Spain.
  • Sánchez-Durán N; Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA) S. A, Avda. Richard Grandío s/n, 33193, Oviedo, Spain.
  • Capín R; Instituto de Medicina Oncológica y Molecular de Asturias (IMOMA) S. A, Avda. Richard Grandío s/n, 33193, Oviedo, Spain.
  • Plasencia A; Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Viejo-Díaz M; Hospital Universitario Central de Asturias, Oviedo, Spain.
  • García-González N; Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Hernando I; Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Llorente JL; Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Repáraz-Andrade A; Hospital Álvaro Cunqueiro, Vigo, Spain.
  • Torreira-Banzas C; Hospital Álvaro Cunqueiro, Vigo, Spain.
  • Rosell J; Hospital Universitario Son Espases, Palma de Mallorca, Spain.
  • Govea N; Hospital Universitario Son Espases, Palma de Mallorca, Spain.
  • Gómez-Martínez JR; Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Núñez-Batalla F; Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Garrote JA; Hospital Universitario Río Hortega, Valladolid, Spain.
  • Mazón-Gutiérrez Á; Hospital Universitario Marqués de Valdecilla, Santander, Spain.
  • Costales M; Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Isidoro-García M; Hospital Universitario Marqués de Valdecilla, Santander, Spain.
  • García-Berrocal B; Instituto de Investigación Biomédica de Salamanca, Salamanca, Spain.
  • Ordóñez GR; Instituto de Investigación Biomédica de Salamanca, Salamanca, Spain.
  • Cadiñanos J; Disease Research And Medicine (DREAMgenics) S. L., Oviedo, Spain.
BMC Med Genomics ; 11(1): 58, 2018 Jul 09.
Article in En | MEDLINE | ID: mdl-29986705

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genomics / Hearing Loss Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Country/Region as subject: Europa Language: En Journal: BMC Med Genomics Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: España Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genomics / Hearing Loss Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Country/Region as subject: Europa Language: En Journal: BMC Med Genomics Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: España Country of publication: Reino Unido