11 results on '"GJB6"'
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2. A recurrent mutation of GJB6 in a big Chinese family with Hidrotic ectodermal dysplasia
3. Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes’ clinical diagnostics
4. Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects
5. Analysis of the presence of the GJB6 mutations in patients heterozygous for GJB2 mutation in Brazil
6. Identification of four novel connexin 26 mutations in non-syndromic deaf patients: genotype–phenotype analysis in moderate cases
7. Molecular Cloning and Evolutionary Analysis of GJB6 in Mammals
8. Mutation analysis of GJB2 and GJB6 genes in Southeastern Brazilians with hereditary nonsyndromic deafness
9. GJB2 and GJB6 gene mutations found in Indian probands with congenital hearing impairment
10. Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy
11. The c.IVS1+1G>A mutation intheGJB2 gene is prevalent and large deletions involving theGJB6 gene are not present in the Turkish population
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