Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb03377.x/fullpdf
Reference11 articles.
1. Multipoint linkage of 9 anonymous probes to HPRT, Factor 9, and Fragile X;Brown;Am. J. Med. Genet.,1988
2. The genetic linkage map of the human chromosome;Drayna;Science,1985
3. X-linked lymphoprolifer-ative syndrome. Identification of a large family in Switzerland;Hayoz;Am. J. Med.,1988
4. Strategies for multilocus linkage analysis in humans;Lathrop;Proc. Natl. Acad. Sci. USA,1984
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1. X-linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible male;Clinical Genetics;2008-06-28
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3. A Spectrum of Mutations in SH2D1A That Causes X-linked Lymphoproliferative Disease and Other Epstein-Barr Virus-associated Illnesses;Leukemia & Lymphoma;2002-01
4. Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease;European Journal of Pediatrics;1994-06
5. Epstein-Barr Virus In B Lymphocytes: Viral Gene Expression and Function in Latency;Advances in Cancer Research;1992
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