The molecular basis of X-linked immunodeficiency disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799623
Reference27 articles.
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3. Francke U, Ochs HD, Darras BT, Swaroop A (1990) Origin of mutations in two families with X-linked chronic granulomatous disease.Blood 76: 602–606.
4. Goodship J, Malcolm S, Lau YL, Pembrey ME, Levinsky RJ (1988) Use of X-chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiency.Lancet 1, 729–730.
5. Goodship J, Levinsky RJ, Malcolm S (1989) Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male.Hum Genet 84: 11–14.
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2. GENE THERAPY FOR CONGENITAL IMMUNODEFICIENCY DISEASES;Immunology and Allergy Clinics of North America;1996-05
3. GENE THERAPY FOR CONGENITAL IMMUNODEFICIENCY DISEASES;Radiologic Clinics of North America;1996-05
4. Distinction between gamma c detection and function in YT lymphoid cells and in the granulocyte-macrophage colony-stimulating factor-responsive human myeloid cell line, Tf-1;Blood;1995-12-15
5. X-linked severe combined immunodeficiency disease and the gamma c receptor component: prospects for molecular diagnosis;Clinical Diagnostic Laboratory Immunology;1995-09
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