Literature DB >> 13828799

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

J B GRAHAM.   

Abstract

Entities:  

Keywords:  KIDNEY DISEASES/genetics

Mesh：

Year:  1959        PMID： 13828799      PMCID： PMC1932036     

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


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  9 in total

1.  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

2.  Further scoring types in sequential linkage tests, with a critical review of autosomal and partial sex linkage in man.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1957-03       Impact factor: 11.025

3.  Hereditary renal disease associated with nerve deafness and ocular lesions.

Authors:  R B GOLDBLOOM; F C FRASER; D WAUGH; M ARONOVITCH; F W WIGLESWORTH
Journal:  Pediatrics       Date:  1957-08       Impact factor: 7.124

4.  Hereditary factors in chronic Bright's disease; a study of two affected kindreds.

Authors:  E D ROBIN; F H GARDNER; S A LEVINE
Journal:  Trans Assoc Am Physicians       Date:  1957

5.  [Familial syndrome of nephropathy with deafness].

Authors:  J HAMBURGER; J CROSNIER; J LISSAC; J NAFFAH
Journal:  J Urol Medicale Chir       Date:  1956-03

6.  Hereditary hematuria, nephropathy and deafness; preliminary report.

Authors:  G S STURTZ; E C BURKE
Journal:  N Engl J Med       Date:  1956-06-14       Impact factor: 91.245

7.  Congenital hereditary hematuria.

Authors:  G C REYERSBACH; A M BUTLER
Journal:  N Engl J Med       Date:  1954-09-02       Impact factor: 91.245

8.  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

9.  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
  9 in total
  11 in total

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

Authors:  M M COHEN; G CASSADY; B L HANNA
Journal:  Am J Hum Genet       Date:  1961-12       Impact factor: 11.025

2.  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

3.  Abnormal Segregation in Hereditary Renal Disease with Deafness.

Authors:  R F Shaw; R A Glover
Journal:  Am J Hum Genet       Date:  1961-03       Impact factor: 11.025

Review 4.  Alport's syndrome.

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

Review 5.  The application of molecular biology to the prenatal diagnosis of renal disease.

Authors:  F A Flinter; M Bobrow
Journal:  Pediatr Nephrol       Date:  1988-07       Impact factor: 3.714

6.  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

7.  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

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

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

9.  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

10.  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
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