Regular ArticleA Second Family with Nonsyndromic Sensorineural Hearing Loss Linked to Xp21.2: Refinement of the DFN4 Locus within DMD☆
References (48)
- et al.
Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach
Genomics
(1992) - et al.
A linkage map of microsatellite markers on the human X chromosome
Genomics
(1994) - et al.
Extra-muscle involvement in dystrophinopathies: An electroretinography and evoked potential study
J. Neurol. Sci.
(1997) - et al.
A yeast artificial chromosome contig containing the complete Duchenne muscular dystrophy gene
Genomics
(1992) - et al.
Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy
Opthalmology
(1994) - et al.
Reversible contraction of isolated mammalian cochlear hair cells
Hear. Res.
(1985) - et al.
The structural and functional diversity of dystrophin
Nat. Genet.
(1993) Hearing acuity in patients with muscular dystrophy
Dev. Med. Child. Neurol.
(1973)- et al.
Use of cyclosporin A in establishing Epstein–Barr virus transformed human lymphoblastoid cell lines
In Vitro
(1984) - et al.
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
Hum. Genet.
(1990)
Evoked mechanical responses of isolated cochlear outer hair cells
Science
(1985)
An alternative dystrophin transcript specific to peripheral nerve
Nat. Genet.
(1993)
Multiplex PCR for the diagnosis of Duchenne muscular dystrophy
PCR Protocols: A Guide to Methods and Applications
(1990)
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms
Am. J. Hum. Genet.
(1991)
Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype
Br. J. Ophthalmol.
(1994)
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
Science
(1995)
A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22
Hum. Mol. Genet.
(1996)
A comprehensive genetic map of the human genome based on 5,264 microsatellites
Nature
(1996)
Dystrophin expression in the hair cells of the cochlea
J. Neurocytol.
(1995)
Clinical molecular diagnostics
Current Protocols in Human Genetics,
(1994)
A novel dystrophin isoform is required for normal retinal electrophysiology
Hum. Mol. Genet.
(1995)
Rapid detection of CA polymorphisms in cloned DNA: Application to the 5′ region of the dystrophin gene
Am. J. Hum. Genet.
(1991)
Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness
Ann. Hum. Genet.
(1965)
Cited by (0)
- ☆
M. A. InnisD. H. GelfandJ. J. SninskyT. J. White
- 1
To whom correspondence should be addressed at the Laboratory of Molecular Otology, Epstein Laboratories, University of California San Francisco, 533 Parnassus Avenue, Room U490A, San Francisco, CA 94143-0526. Telephone: (415) 476-4880. Fax: (415) 476-2169. E-mail:[email protected].
Copyright © 1998 Academic Press. All rights reserved.