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Literature DB >> 2567696

Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37.

J C Skare¹, H L Grierson, J L Sullivan, R L Nussbaum, D T Purtilo, B S Sylla, G M Lenoir, D S Reilly, B N White, A Milunsky.

Abstract

Analysis of seven kindreds indicates that the XLP locus exhibits 1% recombination with DXS42 (lod = 17.5) and no recombination with DXS37 (lod = 13.3).

Entities: Disease Gene

Mesh：

Substances：
Genetic Markers

Year: 1989 PMID： 2567696 DOI： 10.1007/BF00273997

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

14 in total

1. Report of the Committee on Methods of Linkage Analysis and Reporting.

Authors: P M Conneally; J H Edwards; K K Kidd; J M Lalouel; N E Morton; J Ott; R White
Journal: Cytogenet Cell Genet Date: 1985

2. A fatal x-linked recessive reticuloendothelial syndrome with hyperglobulinemia. X-linked recessive reticuloendotheliosis.

Authors: J M Falletta; D J Fernbach; D B Singer; M A South; B H Landing; C W Heath; N A Shore; F F Barrett
Journal: J Pediatr Date: 1973-10 Impact factor: 4.406

3. Pathogenesis and phenotypes of an X-linked recessive lymphoproliferative syndrome.

Authors: D T Purtilo
Journal: Lancet Date: 1976-10-23 Impact factor: 79.321

4. A strategy to reveal high-frequency RFLPs along the human X chromosome.

Authors: J Aldridge; L Kunkel; G Bruns; U Tantravahi; M Lalande; T Brewster; E Moreau; M Wilson; W Bromley; T Roderick
Journal: Am J Hum Genet Date: 1984-05 Impact factor: 11.025

5. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

Authors: L M Mulligan; M A Phillips; C J Forster-Gibson; J Beckett; M W Partington; N E Simpson; J J Holden; B N White
Journal: Am J Hum Genet Date: 1985-05 Impact factor: 11.025

6. Malignant lymphoma of the small intestine in multiple family members: association with an immunologic deficiency.

Authors: H S Maurer; S P Gotoff; L Allen; J Bolan
Journal: Cancer Date: 1976-05 Impact factor: 6.860

7. Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq.

Authors: J C Skare; J L Sullivan; A Milunsky
Journal: Hum Genet Date: 1989-07 Impact factor: 4.132

8. Strategies for multilocus linkage analysis in humans.

Authors: G M Lathrop; J M Lalouel; C Julier; J Ott
Journal: Proc Natl Acad Sci U S A Date: 1984-06 Impact factor: 11.205

9. Mapping the X-linked lymphoproliferative syndrome.

Authors: J C Skare; A Milunsky; K S Byron; J L Sullivan
Journal: Proc Natl Acad Sci U S A Date: 1987-04 Impact factor: 11.205

10. Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment.

Authors: D S Reilly; R A Lewis; D H Ledbetter; R L Nussbaum
Journal: Am J Hum Genet Date: 1988-05 Impact factor: 11.025

13 in total

Review 1. Genetics of human X-linked immunodeficiency diseases.

Authors: R W Hendriks; R K Schuurman
Journal: Clin Exp Immunol Date: 1991-08 Impact factor: 4.330

Review 2. X-linked lymphoproliferative disease (XLP) as a model of Epstein-Barr virus-induced immunopathology.

Authors: D T Purtilo
Journal: Springer Semin Immunopathol Date: 1991

3. Fine structure mapping of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene region of the human X chromosome (Xq26).

Authors: J A Nicklas; T C Hunter; J P O'Neill; R J Albertini
Journal: Am J Hum Genet Date: 1991-08 Impact factor: 11.025

Review 8. Epstein-Barr virus infection and associated diseases in children. I. Pathogenesis, epidemiology and clinical aspects.

Authors: V Schuster; H W Kreth
Journal: Eur J Pediatr Date: 1992-10 Impact factor: 3.183

Review 9. Immune regulation in Epstein-Barr virus-associated diseases.

Authors: R Khanna; S R Burrows; D J Moss
Journal: Microbiol Rev Date: 1995-09

10. Epstein-Barr virus infection rapidly progressing to monoclonal lymphoproliferative disease in a child with selective immunodeficiency.

Authors: V Schuster; H W Kreth; H K Müller-Hermelink; H I Huppertz; A C Feller; D Neumann-Haefelin; H Wiegand; N Müller-Lantzsch
Journal: Eur J Pediatr Date: 1990-11 Impact factor: 3.183