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Literature DB >> 17948465

Abnormal Segregation in Hereditary Renal Disease with Deafness.

R F Shaw, R A Glover.

Abstract

Entities: Disease

Year: 1961 PMID： 17948465 PMCID： PMC1932106

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

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15 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. [Cytological principles of heredity relatively connected to sex in mammals].

Authors: R MATTHEY
Journal: Experientia Date: 1957-09-15

3. 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

4. Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome.

Authors: E SOHAR
Journal: AMA Arch Intern Med Date: 1956-05

5. 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

6. Syndrome of hereditary hematuria, nephropathy and deafness.

Authors: G S STURTZ; E C BURKE
Journal: Proc Staff Meet Mayo Clin Date: 1958-05-28

7. [Familial syndrome of nephropathy with deafness].

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

8. The chromosomes of man.

Authors: C E FORD; J L HAMERTON
Journal: Nature Date: 1956-11-10 Impact factor: 49.962

9. 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

10. Congenital hereditary hematuria.

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

20 in total

1. Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.

Authors: R S Ozen; B E Baysal; B Devlin; J E Farr; M Gorry; G D Ehrlich; C W Richard
Journal: Am J Hum Genet Date: 1999-06 Impact factor: 11.025

2. 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

Review 3. 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

4. Causes of sex ratio bias may account for unisexual sterility in hybrids: a new explanation of Haldane's rule and related phenomena.

Authors: L D Hurst; A Pomiankowski
Journal: Genetics Date: 1991-08 Impact factor: 4.562

5. Problem of sex ratio in cases of type I syndactyly.

Authors: C M Woolf; D L Cone
Journal: J Med Genet Date: 1977-04 Impact factor: 6.318

6. Meiotic drive at the myotonic dystrophy and the cone-rod dystrophy loci on chromosome 19q13.3.

Authors: C F Inglehearn; C Y Gregory
Journal: Am J Hum Genet Date: 1997-06 Impact factor: 11.025

Review 7. Alport's syndrome.

Authors: F Flinter
Journal: J Med Genet Date: 1997-04 Impact factor: 6.318

Review 8. Alport's syndrome.

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

Review 9. Genetics of Alport's syndrome.

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

10. 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