Literature DB >> 7395871

Estimation of male to female ratio of mutation rates from carrier-detection tests in X-linked disorders.

R M Winter.   

Abstract

A method is presented for the estimation of the ratio of male to female mutation rates from female carrier-detection test data from pedigrees containing an isolated male manifesting an X-linked necessive disorder. Pedigrees of any size and complexity (barring consanguinity) and containing any number of tested females can be utilized. The relative fitness of affected males and carrier females, and the segregation probability of the abnormal gamete in females, can be estimated simultaneously with the ratio of mutation rates in order to test specific hypotheses against given bodies of data. Here this method is applied to families containing isolated individuals affected with Lesch-Nyhan syndrome.

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Mesh:

Year:  1980        PMID: 7395871      PMCID: PMC1686120     

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


  14 in total

1.  Carrier detection in Duchenne muscular dystrophy.

Authors:  A D Roses; M J Roses; S E Miller; K L Hull; S H Appel
Journal:  N Engl J Med       Date:  1976-01-22       Impact factor: 91.245

2.  Answer to criticism of Morton and Lalouel.

Authors:  U Francke; J Felsenstein; S M Gartler; W L Nyhan; J E Seegmiller
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

3.  Spontaneous frequencies of point mutations in mice.

Authors:  A G Searle
Journal:  Humangenetik       Date:  1972

4.  Systemic membrane defect in the proximal muscular dystrophies.

Authors:  N A Pickard; H D Gruemer; H L Verrill; E R Isaacs; M Robinow; W E Nance; E C Myers; B Goldsmith
Journal:  N Engl J Med       Date:  1978-10-19       Impact factor: 91.245

Review 5.  Spontaneous mutation in man.

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

6.  Use of overlapping normal distributions in genetic counselling.

Authors:  N R Dennis; C O Carter
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318

7.  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

8.  Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy.

Authors:  A M Davie; A E Emery
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

9.  The sporadic case of haemophilia A.

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

10.  The laboratory diagnosis of the carrier state for classic hemophilia.

Authors:  O D Ratnoff; P K Jones
Journal:  Ann Intern Med       Date:  1977-05       Impact factor: 25.391

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  8 in total

1.  Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.

Authors:  A H Bröcker-Vriends; F R Rosendaal; J C van Houwelingen; E Bakker; G J van Ommen; J J van de Kamp; E Briët
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

2.  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

3.  Recurrent mutation pressure does not explain the prevalence of the marker (X) syndrome.

Authors:  F Vogel; J Krüger; K B Nielsen; J P Fryns; D Schindler; A Schinzel; A Schmidt; E Schwinger
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

4.  Germ-line origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutation.

Authors:  R P Ketterling; E Vielhaber; C D Bottema; D J Schaid; M P Cohen; C L Sexauer; S S Sommer
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

Review 5.  Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.

Authors:  H Moser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis.

Authors:  F R Rosendaal; A H Bröcker-Vriends; J C van Houwelingen; C Smit; I Varekamp; H van Dijck; T P Suurmeijer; J P Vandenbroucke; E Briët
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

7.  A maximum likelihood estimate of the sex ratio of mutation rates in haemophilia A.

Authors:  R M Winter; E G Tuddenham; E Goldman; K B Matthews
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Authors:  E Bakker; E J Bonten; L F De Lange; H Veenema; D Majoor-Krakauer; M H Hofker; G J Van Ommen; P L Pearson
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

  8 in total

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