Abstract |
The Xq22 region of the human X chromosome contains genes for a number of inherited disorders. Sixty-nine yeast artificial chromosome clones have been isolated and assembled into a 6.5-Mb contig that contains 33 DNA markers localized to this region. This contig extends distally from DXS366 to beyond DXS87 and includes the genes involved in X-linked agammaglobulinemia (btk), Fabry disease (GLA), and Pelizaeus-Merzbacher disease (PLP). The order of markers in this contig is consistent with the known genetic and physical mapping information of Xq22. This cloned material provides a source from which to isolate other genes located in this part of the X chromosome.
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Authors | D Vetrie, E Kendall, A Coffey, S Hassock, J Collins, C Todd, H Lehrach, M Bobrow, D R Bentley, A Harris |
Journal | Genomics
(Genomics)
Vol. 19
Issue 1
Pg. 42-7
(Jan 01 1994)
ISSN: 0888-7543 [Print] United States |
PMID | 8188239
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adult
- Agammaglobulinemia
(genetics)
- Chromosome Walking
- Chromosomes, Artificial, Yeast
- Diffuse Cerebral Sclerosis of Schilder
(genetics)
- Fabry Disease
(genetics)
- Gene Library
- Genetic Markers
- Humans
- X Chromosome
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