Literature DB >> 868880

A probable sex difference in some mutation rates.

F Vogel.   

Abstract

Mesh:

Year:  1977        PMID: 868880      PMCID: PMC1685321     

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


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  22 in total

1.  Muscular dystrophy in Northern Ireland, I. An account of the condition in fifty-one families.

Authors:  A C STEVENSON
Journal:  Ann Eugen       Date:  1953-06

2.  Genetic epidemiology of Lesch-Nyhan disease.

Authors:  N E Morton; J M Lalouel
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

Review 3.  [New data on the genetics and classification of muscular dystrophies].

Authors:  P E Becker
Journal:  Humangenetik       Date:  1972

4.  Spontaneous frequencies of point mutations in mice.

Authors:  A G Searle
Journal:  Humangenetik       Date:  1972

5.  The effect of parental age on rates of mutation for hemophilia and evidence for differing mutation rates for hemophilia A and B.

Authors:  I Barrai; H M Cann; L L Cavalli-Sforza; P De Nicola
Journal:  Am J Hum Genet       Date:  1968-05       Impact factor: 11.025

Review 6.  Spontaneous mutation in man.

Authors:  F Vogel; R Rathenberg
Journal:  Adv Hum Genet       Date:  1975

7.  [The effect of the age of the father at conception on the mutations to hemphilia A].

Authors:  J Herrmann
Journal:  Humangenetik       Date:  1966

8.  [Are the mutation rates for the X-chromosomal forms of hemophilia in female gonads lower than in the gonads of males?].

Authors:  F Vogel
Journal:  Humangenetik       Date:  1965

9.  The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease.

Authors:  U Francke; J Felsenstein; S M Gartler; B R Migeon; J Dancis; J E Seegmiller; F Bakay; W L Nyhan
Journal:  Am J Hum Genet       Date:  1976-03       Impact factor: 11.025

10.  The sporadic case of haemophilia A.

Authors:  R Biggs; C R Rizza
Journal:  Lancet       Date:  1976-08-28       Impact factor: 79.321

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  26 in total

1.  High male:female ratio of germ-line mutations: an alternative explanation for postulated gestational lethality in males in X-linked dominant disorders.

Authors:  G H Thomas
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Segregation analysis of hemophilia A and B.

Authors:  I Barrai; H M Cann; L L Cavalli-Sforza
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

3.  Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe.

Authors:  D Sinnett; L Lavergne; S B Melançon; L Dallaire; M Potier; D Labuda
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

4.  Segregation analysis of hemophilia A and B.

Authors:  I Barrai; H M Cann; L L Cavalli-Sforza; G Barbujani; P De Nicola
Journal:  Am J Hum Genet       Date:  1985-07       Impact factor: 11.025

5.  Advancing paternal age and psychiatric disorders.

Authors:  Emma Frans; James H MacCabe; Abraham Reichenberg
Journal:  World Psychiatry       Date:  2015-02       Impact factor: 49.548

6.  On the power to detect differences between male and female mutation rates for Duchenne muscular dystrophy, using classical segregation analysis and restriction fragment length polymorphisms.

Authors:  E R Karel; G J te Meerman; L P Ten Kate
Journal:  Am J Hum Genet       Date:  1986-06       Impact factor: 11.025

7.  Somatic mosaicism in hemophilia A: a fairly common event.

Authors:  M Leuer; J Oldenburg; J M Lavergne; M Ludwig; A Fregin; A Eigel; R Ljung; A Goodeve; I Peake; K Olek
Journal:  Am J Hum Genet       Date:  2001-06-14       Impact factor: 11.025

8.  Duchenne muscular dystrophy. Frequency of sporadic cases.

Authors:  G A Danieli; G Barbujani
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Genetics of neurofibromatosis 1 in Japan: mutation rate and paternal age effect.

Authors:  T Takano; T Kawashima; Y Yamanouchi; K Kitayama; T Baba; K Ueno; H Hamaguchi
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

10.  A probable sex difference in mutation rates in ornithine transcarbamylase deficiency.

Authors:  C Bonaïti-Pellié; A Pelet; H Ogier; J R Nelson; C Largillière; J Berthelot; J M Saudubray; A Munnich
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

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