Guidelines and recommendations for testing of Cx26 mutations and interpretation of results
Autor: | A. Read, V. Newton, Alessandra Murgia, Agnete Parving, Paolo Gasparini, M. Mazzoli, M. Bitner-Glindzicz |
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Přispěvatelé: | Mazzoli, M, Newton, V, Murgia, A, BITNER GLINDZICZ, M, Gasparini, Paolo, Read, A, Parving, A. |
Rok vydání: | 2004 |
Předmět: |
Adolescent
Hearing loss Bioinformatics Connexins medicine Humans Genetic Testing Child Hearing Loss Genetic testing medicine.diagnostic_test business.industry Interpretation (philosophy) Infant Newborn Infant General Medicine Infant newborn Connexin 26 Europe Otorhinolaryngology Child Preschool Pediatrics Perinatology and Child Health Mutation (genetic algorithm) Mutation medicine.symptom business |
Zdroj: | International journal of pediatric otorhinolaryngology. 68(11) |
ISSN: | 0165-5876 |
Databáze: | OpenAIRE |
Externí odkaz: |