Literature DB >> 1683204

Molecular genetics of X-linked hearing impairment.

H G Brunner1, B Smeets, D Smeets, M Nelen, C W Cremers, H H Ropers.   

Abstract

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Year:  1991        PMID： 1683204     DOI： 10.1111/j.1749-6632.1991.tb19586.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN： 0077-8923            Impact factor:   5.691


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  3 in total

1.  Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3).

Authors:  I Bach; H G Brunner; P Beighton; R H Ruvalcaba; W Reardon; M E Pembrey; S D van der Velde-Visser; G A Bruns; C W Cremers; F P Cremers
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

2.  Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

Authors:  B Bonné-Tamir; A L DeStefano; C E Briggs; R Adair; B Franklyn; S Weiss; M Korostishevsky; M Frydman; C T Baldwin; L A Farrer
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

3.  A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

Authors:  L Tranebjaerg; C Schwartz; H Eriksen; S Andreasson; V Ponjavic; A Dahl; R E Stevenson; M May; F Arena; D Barker
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318
  3 in total

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