Literature DB >> 7835091

Fine deletion mapping of the p22 region of the human X chromosome using a radiation-induced hybrid panel.

S Heuertz1, A Smahi, M Sanak, L Holvoet-Vermaut, M C Hors-Cayla.   

Abstract

Radiation-induced somatic cell hybrids containing fragments of the human X chromosome were constructed. A panel of 17 hybrids was selected with the help of known markers in the Xp22 region. These hybrids identified 11 different breakpoints between Xp22.2 and Xp21.3. Eight markers were located in eight of the nine corresponding intervals, resulting in the following physical map: tel...DXS89-DXS278-DXS85-(DXS1224, DXS16)-(GLRA2, DXS987)-DXS207-(DXS-197, DXS1053)-(DXS43, DXS1195)-(DXS1229, DXS-999)-(DXS1052, DXS92, DXS274)-(DXS41, DXS1226)-DXS1198-DXS28...cen.

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Year:  1995        PMID: 7835091     DOI: 10.1159/000133926

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  1 in total

1.  Genetic mapping of Xp22.12-p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL).

Authors:  S Heuertz; A Smahi; A O Wilkie; M Le Merrer; P Maroteaux; M C Hors-Cayla
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

  1 in total

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