Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq
- 1 July 1989
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 82 (4) , 349-353
- https://doi.org/10.1007/bf00273996
Abstract
The X-linked lymphoproliferative syndrome (XLP) results in fatal infectious mononucleosis, hypogammaglobulinemia, and malignant lymphoma. The mutation has been mapped relative to several restriction fragment length polymorphism (RFLP) markers in the X121-Xq27 vicinity. The DXS37 locus was found to be near both the DXS42 and XLP loci.This publication has 13 references indexed in Scilit:
- Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile XAmerican Journal of Medical Genetics, 1988
- Genetic mapping of nine DNA markers in the q11 → q22 region of the human X chromosomeGenomics, 1987
- Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26?q27Human Genetics, 1987
- Mapping the X-linked lymphoproliferative syndrome.Proceedings of the National Academy of Sciences, 1987
- A DNA marker closely linked to the factor IX (haemophilia B) geneHuman Genetics, 1987
- RFLP locus DXS42 is proximal to the locus for hypoxanthine phosphoribosyltransferase.1986
- Regional localization of 18 human X-linked DNA sequencesCytogenetic and Genome Research, 1986
- The Genetic Linkage Map of the Human X ChromosomeScience, 1985
- Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qterSomatic Cell and Molecular Genetics, 1984
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences, 1984