Found: 6
Select item for more details and to access through your institution.
Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family.
- Published in:
- Human Genetics, 2003, v. 112, n. 2, p. 156, doi. 10.1007/s00439-002-0833-0
- By:
- Publication type:
- Article
An interlaboratory comparison of ITS2-PCR for the identification of yeasts, using the ABI Prism 310 and CEQ8000 capillary electrophoresis systems.
- Published in:
- BMC Microbiology, 2005, v. 5, p. 14, doi. 10.1186/1471-2180-5-14
- By:
- Publication type:
- Article
Deafness linked to DFNA2: one locus but how many genes?
- Published in:
- Nature Genetics, 1999, v. 21, n. 3, p. 263, doi. 10.1038/6778
- By:
- Publication type:
- Article
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 7, p. 1321, doi. 10.1093/hmg/8.7.1321
- By:
- Publication type:
- Article
Two frequent missense mutations in Pendred syndrome.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 7, p. 1099, doi. 10.1093/hmg/7.7.1099
- By:
- Publication type:
- Article
Nonsyndromic Autosomal Dominant Progressive Sensorineural Hearing Loss: Audiologic Analysis of a Pedigree Linked to DFNA2.
- Published in:
- Laryngoscope, 1998, v. 108, n. 1, p. 74, doi. 10.1097/00005537-199801000-00014
- By:
- Publication type:
- Article