Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome-Reference-Cited by-同舟云学术

Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome

Published:1990-03 Issue:3 Volume:6 Page:568-571
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Greer W.L.,Somani A.-K.,Kwong P.C.,Peacocke M.,Rubin L.A.,Siminovitch K.A.

Publisher

Elsevier BV

Subject

Genetics

Reference26 articles.

1. Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea;Aldrich;Paediatrics,1954

2. A strategy to reveal high-frequency RFLPs along the human X-chromosome;Aldridge;Amer. J. Hum. Genet,1984

3. A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12;Arveiler;Nucleic Acids Res,1987

4. The Wiskott-Aldrich syndrome: An immunologic deficiency disease involving the afferent limb of immunity;Cooper;Amer. J. Med,1968

5. RFLP detected by an X-linked cDNA encoding EPA/TIMP;Durfy;Nucleic Acids Res,1986

Cited by 25 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prenatal diagnosis and genetic analysis of Wiskott-Aldrich syndrome;Prenatal Diagnosis;2003

2. Spontaneous In Vivo Reversion of an Inherited Mutation in the Wiskott-Aldrich Syndrome;The Journal of Immunology;2001-04-15

3. The Wiskott-Aldrich syndrome;Springer Seminars in Immunopathology;1998

4. 3. Molecular Basis for X-Linked Immunodeficiencies;Advances in Genetics;1997

5. Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus;Human Molecular Genetics;1995-07-01