Found: 17
Select item for more details and to access through your institution.
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.
- Published in:
- Clinical Genetics, 2008, v. 74, n. 3, p. 223, doi. 10.1111/j.1399-0004.2008.01053.x
- By:
- Publication type:
- Article
The frequency of GJB2 mutations and the Δ (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population.
- Published in:
- 2004
- By:
- Publication type:
- Letter
Haplotype analysis of the USH1D locus and genotype–phenotype correlations.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 1, p. 58, doi. 10.1034/j.1399-0004.2001.600109.x
- By:
- Publication type:
- Article
Standards for ethical publication.
- Published in:
- 2007
- By:
- Publication type:
- Journal Article
Hearing genes and cisplatin deafness: a pilot study.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Hearing loss in Union Army veterans from 1862-1920.
- Published in:
- 2004
- By:
- Publication type:
- Journal Article
Spastic diplegia and other motor disturbances in infants receiving interferon-alpha.
- Published in:
- 2004
- By:
- Publication type:
- Journal Article
Age-related mitochondrial DNA mutations in the human larynx.
- Published in:
- 2000
- By:
- Publication type:
- Journal Article
Temporal bone histopathology in connexin 26-related hearing loss.
- Published in:
- 2000
- By:
- Publication type:
- journal article
Laryngomalacia and its treatment.
- Published in:
- 1999
- By:
- Publication type:
- Journal Article
Laryngeal motion during exercise.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Commentary on 'Dysplasia in adults with recurrent respiratory papillomatosis: incidence and risk factors'.
- Published in:
- 2009
- By:
- Publication type:
- Journal Article
Book reviews.
- Published in:
- 2007
- By:
- Publication type:
- Journal Article
Case of progressive dysplasia concomitant with intralesional codifovir administration for recurrent respiratory papillomatosis.
- Published in:
- 2005
- By:
- Publication type:
- Journal Article
New treatment options for lymphangioma in infants and children.
- Published in:
- 2002
- By:
- Publication type:
- Journal Article
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss.
- Published in:
- Human Mutation, 1998, v. 11, n. 5, p. 387, doi. 10.1002/(SICI)1098-1004(1998)11:5<387::AID-HUMU6>3.0.CO;2-8
- By:
- Publication type:
- Article
Editorial. Standards for ethical publication.
- Published in:
- 2006
- By:
- Publication type:
- Journal Article