Your browser doesn't support javascript.
loading
Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients.
Marková, Simona; Safka Brozková, Dana; Mészárosová, Anna; Neupauerová, Jana; Groh, Daniel; Krecková, Gabriela; Lassuthová, Petra; Seeman, Pavel.
Afiliación
  • Marková S; DNA Laboratory, Department of Paediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital. Electronic address: simona.markova@protonmail.ch.
  • Safka Brozková D; DNA Laboratory, Department of Paediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital.
  • Mészárosová A; DNA Laboratory, Department of Paediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital.
  • Neupauerová J; DNA Laboratory, Department of Paediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital.
  • Groh D; Otorinolaryngology Centrum, FORTMEDICA, Prague, Czech Republic.
  • Krecková G; Centre for Medical Genetics and Reproductive Medicine GENNET, Prague, Czech Republic.
  • Lassuthová P; DNA Laboratory, Department of Paediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital.
  • Seeman P; DNA Laboratory, Department of Paediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital.
Int J Pediatr Otorhinolaryngol ; 86: 27-33, 2016 Jul.
Article en En | MEDLINE | ID: mdl-27260575
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Pérdida Auditiva Sensorineural / Mutación Límite: Adult / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Int J Pediatr Otorhinolaryngol Año: 2016 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: Predisposición Genética a la Enfermedad / Pérdida Auditiva Sensorineural / Mutación Límite: Adult / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Int J Pediatr Otorhinolaryngol Año: 2016 Tipo del documento: Article