Literature DB >> 2902796

Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.

W T Brown1, W Ye, A C Gross, C B Chan, C S Dobkin, E C Jenkins.   

Abstract

We have analyzed the segregation of restriction fragment length polymorphisms (RFLPs) associated with 9 anonymous probes detecting loci DXS10, DXS15, DXS19, DXS37, DXS51, DXS52, DXS98, DXS99, and DXS100 and probes for HPRT and F9 in a set of 40 families segregating fragile X (fra(X]. Using two-point and multipoint analysis, we have established their relative genetic locations. The results indicate that DXS99 and DXS10, unlike previous reports, are not tightly linked to F9. A new locus was found to map within the F9 - fra(X) region. DXS98 showed 6% recombination with fra(X) and appeared to be the closest locus to fra(X). These results will be useful for mapping the relative position of newly defined X probes in this region and for future genetic studies of families with fra(X), hemophilia B, or Lesch-Nyhan mutations.

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Year:  1988        PMID: 2902796     DOI: 10.1002/ajmg.1320300157

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  Fine structure mapping of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene region of the human X chromosome (Xq26).

Authors:  J A Nicklas; T C Hunter; J P O'Neill; R J Albertini
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

2.  New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.

Authors:  R E Schnur; S A Ledbetter; D H Ledbetter; D E Merry; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-02       Impact factor: 11.025

3.  Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq.

Authors:  J C Skare; J L Sullivan; A Milunsky
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

4.  Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I.

Authors:  Y Shiloh; G Litvak; Y Ziv; T Lehner; L Sandkuyl; M Hildesheimer; V Buchris; F P Cremers; P Szabo; B N White
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

  4 in total

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