X-linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible male
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03143.x/fullpdf
Reference24 articles.
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2. Centre d'Etude du Polymorphisme Humain (CEPH): collaborative genetic mapping of the human genome;Dausset;Genomics,1990
3. A fatal X-linked recessive reticuloendothelial syndrome with hyperglobulinemia;Falletta;J Pediatr,1973
4. Allogeneic bone marrow transplantation for X-linked lymphoproliferative syndrome;Filipovich;Transplantation,1986
5. Characterisation of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) loci;Gedeon;Am J Med Genet,1992
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1. X;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
2. A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255.;Journal of Medical Genetics;1995-09-01
3. Prenatal diagnosis of X linked lymphoproliferative disease using multiplex polymerase chain reaction.;Journal of Medical Genetics;1995-09-01
4. Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease;European Journal of Pediatrics;1994-06
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