Literature DB >> 3995787

Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis.

H M Kingston, M Sarfarazi, R G Newcombe, N Willis, P S Harper.   

Abstract

Serum creatine kinase levels in 39 control females and 59 obligate carriers of Becker muscular dystrophy (BMD) have been used to construct likelihood ratios for carrier detection. In 24 possible carriers of BMD, analysis of DNA with X chromosome specific DNA probes linked to the dystrophy gene, has been used in conjunction with creatine kinase measurement to calculate final risk estimates of carrier status. Incorporation of information from probe genotype into the Bayesian calculation, enables a substantially lower risk to be deliniated for some possible carriers of the BMD gene. Thus, although the existing DNA probes are not sufficiently closely linked to BMD to be used in prenatal diagnosis, they can make a major contribution to genetic counseling by refining the estimated probability of carrier status.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3995787     DOI: 10.1111/j.1399-0004.1985.tb02280.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  5 in total

1.  A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information.

Authors:  M Sarfarazi; H Williams
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

Review 2.  Diagnosis of genetic disease using recombinant DNA.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

Review 3.  Cardiac involvement in Becker muscular dystrophy.

Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Can J Cardiol       Date:  2008-10       Impact factor: 5.223

4.  Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy.

Authors:  C S Brown; N S Thomas; M Sarfarazi; K E Davies; L Kunkel; P L Pearson; H M Kingston; D J Shaw; P S Harper
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

5.  Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.

Authors:  M Lindlöf; H Kääriäinen; K E Davies; A de la Chapelle
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.