Literature DB >> 2902797

Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).

J Mulley1, G Turner, S Bain, G R Sutherland.   

Abstract

Linkage data using the markers F9, DXS105 (cX55.7), DXS98 (4D-8) and DXS52 (St14) are presented from 22 kindreds segregating with the fragile X. Two-point linkage analysis was carried out taking into account cytogenetic results and penetrance classes defined by mental impairment status of mothers. Recombination frequencies (theta) corresponding to the maximum z scores (z) were obtained between F9 (z = 3.48, theta = 0.18), DXS105 (z = 5.06, theta = 0.07), DXS98 (z = 4.79, theta = 0.01) and DXS52 (z = 6.44, theta = 0.09) and the fragile X. Recombination frequencies between marker loci in fragile X families are also presented. These recombination frequencies need to be combined with those from other studies in order to determine the best estimates of map distances for use in genetic counselling, until markers closer to the fragile X, or at the fragile X, can be used. Most potential fra(X) heterozygotes were informative for flanking markers using the above 4 probes. Carrier risks were determined by 3-point analysis using informative flanking markers, taking into account cytogenetic results. Low level fra(X) expression occurred in 2 probable non-carriers; emphasising the need for extreme caution in the interpretation of low rates of expression.

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Year:  1988        PMID: 2902797     DOI: 10.1002/ajmg.1320300158

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


  6 in total

1.  Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

Authors:  R I Richards; Y Shen; K Holman; H Kozman; V J Hyland; J C Mulley; G R Sutherland
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

2.  Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.

Authors:  V J Hyland; K E Fernandez; D F Callen; R N MacKinnon; E Baker; K Friend; G R Sutherland
Journal:  Hum Genet       Date:  1989-08       Impact factor: 4.132

3.  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

4.  Experience with direct molecular diagnosis of fragile X.

Authors:  J C Mulley; S Yu; A K Gedeon; A Donnelly; G Turner; D Loesch; C J Chapman; R J Gardner; R I Richards; G R Sutherland
Journal:  J Med Genet       Date:  1992-06       Impact factor: 6.318

5.  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

6.  Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).

Authors:  N Dahl; P Goonewardena; H Malmgren; K H Gustavson; G Holmgren; E Seemanova; G Annerén; A Flood; U Pettersson
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

  6 in total

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