Literature DB >> 5865628

Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness.

G R Fraser.   

Abstract

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Year:  1965        PMID： 5865628     DOI： 10.1111/j.1469-1809.1965.tb00512.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


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  10 in total

Review 1.  Genetic deafness.

Authors:  W Reardon
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

Authors:  H G Brunner; A van Bennekom; E M Lambermon; T L Oei; W R Cremers; B Wieringa; H H Ropers
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

3.  Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism.

Authors:  K Fried; M Feinmesser; J Tsitsianov
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

4.  Sex-linked congenital deafness.

Authors:  K N McRae; I A Uchida; M Lewis
Journal:  Am J Hum Genet       Date:  1969-09       Impact factor: 11.025

5.  On the heredity of retinitis pigmentosa.

Authors:  M Jay
Journal:  Br J Ophthalmol       Date:  1982-07       Impact factor: 4.638

6.  Genetic analysis of a group of mentally retarded children.

Authors:  B R Krishnan; A Ramesh; M P Kumari; P M Gopinath
Journal:  Indian J Pediatr       Date:  1989 Mar-Apr       Impact factor: 1.967

7.  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

8.  A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Authors:  A K Lalwani; J R Brister; J Fex; K M Grundfast; A T Pikus; B Ploplis; T San Agustin; H Skarka; E R Wilcox
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

9.  X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.

Authors:  C Piussan; A Hanauer; N Dahl; M Mathieu; C Kolski; V Biancalana; S Heyberger; V Strunski
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

10.  Population genetic studies of retinitis pigmentosa.

Authors:  J A Boughman; P M Conneally; W E Nance
Journal:  Am J Hum Genet       Date:  1980-03       Impact factor: 11.025
  10 in total

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