Literature DB >> 5155309

Genetics of hereditary nephropathy with deafness (Alport's disease).

M Preus, F C Fraser.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5155309     DOI： 10.1111/j.1399-0004.1971.tb00293.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  7 in total

Review 1.  Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.

Authors:  P S Harper
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

Review 2.  Alport's syndrome.

Authors:  M A Crawfurd
Journal:  J Med Genet       Date:  1988-09       Impact factor: 6.318

Review 3.  Genetics of Alport's syndrome.

Authors:  J Feingold; E Bois
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

4.  Mapping of Alport syndrome to the long arm of the X chromosome.

Authors:  C L Atkin; S J Hasstedt; L Menlove; L Cannon; N Kirschner; C Schwartz; K Nguyen; M Skolnick
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

5.  Hereditary nephritis.

Authors:  P V Tishler
Journal:  Br Med J       Date:  1972-11-04

6.  Segregation ratios in Alport's syndrome.

Authors:  E MacNeill; R F Shaw
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

7.  X-linked inheritance of Alport syndrome: family P revisited.

Authors:  S J Hasstedt; C L Atkin
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025
  7 in total

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