Literature DB >> 2897946

DNA polymorphisms, identified by an X-chromosome short-arm probe L 1.28 (DXS7), in different racial groups.

S S Papiha1, S S Bhattacharya, D F Roberts.   

Abstract

Restriction fragment length polymorphisms of the L1.28 probe which is closely linked to X-linked disorders, retinitis pigmentosa and Norrie disease, were studied in samples from England, India and Nigeria. The frequency of the A2 allele (9-kb fragment) was 0.23, 0.55 and 0.46 in England, India and Nigeria, respectively. The differences between the English and Indian populations were highly significant.

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Year:  1988        PMID: 2897946     DOI: 10.1159/000153761

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  2 in total

1.  Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy gene.

Authors:  S S Papiha; D F Roberts; A Clarke; J Burn; D Gardner-Medwin; S S Bhattacharya
Journal:  J Med Genet       Date:  1989-06       Impact factor: 6.318

2.  Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.

Authors:  G de Saint Basile; L D Notarangelo; C Bonaiti-Pellié; M Doussau; O Prolini; I W Craig; A Ugazio; C Griscelli; A Fischer
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

  2 in total

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