Vetrie D, Kendall E, Coffey A, Hassock S, Collins J, Todd C, Lehrach H, Bobrow M, Bentley D R, Harris A
Paediatric Research Unit, United Medical School, London, United Kingdom.
Genomics. 1994 Jan 1;19(1):42-7. doi: 10.1006/geno.1994.1010.
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.