Literature DB >> 13880289

A genetic study of hereditary renal dysfunction with associated nerve deafness.

M M COHEN, G CASSADY, B L HANNA.   

Abstract

Entities:  

Keywords:  DEAFNESS/genetics; KIDNEY DISEASES/genetics

Mesh:

Year:  1961        PMID: 13880289      PMCID: PMC1932137     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  17 in total

1.  Hereditary chronic kidney disease: an alternative to partial sex-linkage in the Utah kindred.

Authors:  J B GRAHAM
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

2.  A follow-up study of hereditary chronic nephritis.

Authors:  G T PERKOFF; C A NUGENT; D A DOLOWITZ; F E STEPHENS; W H CARNES; F H TYLER
Journal:  AMA Arch Intern Med       Date:  1958-11

3.  [Familial chronic bilateral kidney disease].

Authors:  M POLI
Journal:  Helv Med Acta       Date:  1955-05

4.  A heredo-familial syndrome characterized by renal disease, inner ear deafness, and ocular changes.

Authors:  E SOHAR
Journal:  Harefuah       Date:  1954-10-15

5.  Preferential Segregation in Maize.

Authors:  M M Rhoades
Journal:  Genetics       Date:  1942-07       Impact factor: 4.562

6.  Crossing over and Heterochromatin in the X Chromosome of Drosophila Melanogaster.

Authors:  K Mather
Journal:  Genetics       Date:  1939-04       Impact factor: 4.562

7.  Chronic Hereditary Nephritis: Not Shown to be Partially Sex-Linked.

Authors:  J B Graham
Journal:  Am J Hum Genet       Date:  1960-09       Impact factor: 11.025

8.  Chronic Hereditary Nephritis and Y-Chromosome Linkage: Reply to Graham.

Authors:  G T Perkoff; F E Stephens; F H Tyler
Journal:  Am J Hum Genet       Date:  1960-09       Impact factor: 11.025

9.  A clinical study of hereditary interstitial pyelonephritis.

Authors:  G T PERKOFF; F E STEPHENS; D A DOLOWITZ; F H TYLER
Journal:  AMA Arch Intern Med       Date:  1951-08

10.  Partially sex-linked cominant inheritance of interstitial pyelonephritis.

Authors:  F E STEPHENS; G T PERKOFF; D A DOLOWITZ; F H TYLER
Journal:  Am J Hum Genet       Date:  1951-12       Impact factor: 11.025

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  14 in total

Review 1.  Alport's syndrome.

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

2.  Segregation ratios in Alport's syndrome.

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

3.  Correspondence: Alport's syndrome.

Authors:  O Mayo
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

Review 4.  Inherited diseases of the inner ear in man in the light of studies on the mouse.

Authors:  M S Deol
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

5.  A family showing hereditary nephropathy.

Authors:  H Pashayan; F C Fraser; R B Goldbloom
Journal:  Am J Hum Genet       Date:  1971-11       Impact factor: 11.025

6.  [Genetics of the Alport syndrome. Hereditary nephropathy with deafness].

Authors:  J Feingold; E Bois
Journal:  Humangenetik       Date:  1971

7.  Anterior lenticonus and Alport's syndrome.

Authors:  E J Arnott; M D Crawfurd; P J Toghill
Journal:  Br J Ophthalmol       Date:  1966-07       Impact factor: 4.638

8.  Holt-Oram syndrome: clinical and genetic study of a large family.

Authors:  J C Gall; A M Stern; M M Cohen; M S Adams; R T Davidson
Journal:  Am J Hum Genet       Date:  1966-03       Impact factor: 11.025

9.  Charcot-Marie-Tooth disease and nephritis.

Authors:  G Lemieux; J A Neemeh
Journal:  Can Med Assoc J       Date:  1967-11-11       Impact factor: 8.262

10.  Hydrotic ectodermal dysplasia--Clouston's family revisited.

Authors:  M Williams; F C Fraser
Journal:  Can Med Assoc J       Date:  1967-01-07       Impact factor: 8.262

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