Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia-Reference-Cited by-同舟云学术

Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia

Published:1989-10 Issue:3 Volume:83 Page:267-270
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Hendriks R. W.,Mensink E. J. B. M.,Kraakman M. E. M.,Thompson A.,Schuurman R. K. B.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00285169.pdf

Reference27 articles.

1. Bech-Hansen NT, Starozik DM, Dimnik L, Hoar DI, Meschino W (1987) Interstitial deletion and male-gonadal mosaicism as the basis for Duchenne muscular dystrophy. Am J Hum Genet 41:A93

2. Bruton OC (1952) Agammaglobulinemia. Pediatrics 9:722?728

3. Conley ME (1985) B cells in patients with X-linked agammaglobulinemia. J Immunol 134:3070?3074

4. Conley ME, Puck JM (1988) Carrier detection in typical and atypical X-linked agammaglobulinemia. J Pediatr 112:688?694

5. Conley ME, Brown P, Pickard AR, Buckley RH, Miller DS, Raskind WH, Singer JW, Fialkow PJ (1986) Expression of the gene defect in X-linked agammaglobulinemia. N Engl J Med 315:564?567

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1. X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locus;Clinical Genetics;2008-06-28

2. Immunodeficiencies Caused by B-Cell Defects;Molecular Biology of B Cells;2004

3. X-Linked Agammaglobulinemia;Clinical Reviews in Allergy & Immunology;2000

4. Detection of a novel mutation in the SRC homology domain 2 (SH2) of Bruton's tyrosine kinase and direct female carrier evaluation in a family with X-linked agammaglobulinemia;American Journal of Medical Genetics;1996-05-03

5. Female germ line mosaicism as the origin of a unique IL-2 receptor gamma-chain mutation causing X-linked severe combined immunodeficiency.;Journal of Clinical Investigation;1995-02-01