Females with a disorder phenotypically identical to X-linked agammaglobulinemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Link
http://link.springer.com/content/pdf/10.1007/BF00918144.pdf
Reference25 articles.
1. Conley ME, Brown P, Pickard AR, Buckley RH, Miller DS, Raskind WH, Singer JW, Fialkow PJ: Expression of the gene defect in X-linked agammaglobulinemia. N Engl J Med 315:564?567, 1986
2. Fearon ER, Winkelstein JA, Civin CI, Pardoll DM, Vogelstein B: Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation. N Engl J Med 316:427?431, 1987
3. Conley ME, Puck, JM: Carrier detection in typical and atypical X-linked agammaglobulinemia. J Pediat 112:688?694, 1988
4. Hendriks RW, Mensink EJBM, Kraakman MEM, Thompson A, Schuurman RKB: Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia. Hum Genet 83:267?270, 1989
5. Repine JE, Clawson CC, White JG, Holmes B: Spectrum of function of neutrophils from carriers of sex-linked chronic granulomatous disease. J Pediat 87:901?907, 1975
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