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Hledat publikace relevantní k dotazu "DFNB"
DFNB
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Publikace
Studium
publication
Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients
2016 |
2. lékařská fakulta
publication
STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population
2018 |
2. lékařská fakulta
publication
DFNB35 due to a novel mutation in the ESRRB gene in a Czech consanguineous family
2012 |
Ústřední knihovna, 2. lékařská fakulta