Wiskott Aldrich syndrome: an immunodeficiency syndrome not rare in Western Australia
Author:
Publisher
Wiley
Subject
Immunology,Immunology and Allergy,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3038.1993.tb00069.x/fullpdf
Reference79 articles.
1. The Wiskott-Aldrich syndrome in the United States and Canada (1892–1979)
2. 2ER. Stiehm, Immunologie disorders in infants and children . Philadelphia: Saunders, 1989 : 276 -80 .
3. Sex-Linked Hereditary Thrombocytopenia as a Variant of Wiskott–Aldrich Syndrome
4. Familial thrombocytopenia, elevated serum IgA levels and renal disease
5. Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two unrelated males based on studies of maternal T cell X chromosome inactivation [see comments]
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1. Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation;Pediatric Blood & Cancer;2015-04-30
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3. Analysis of clinical and molecular characteristics of Wiskott-Aldrich syndrome in 24 patients from 23 unrelated Chinese families;Pediatric Allergy and Immunology;2010-01-14
4. Clinical and Molecular Characteristics of 35 Chinese Children with Wiskott–Aldrich Syndrome;Journal of Clinical Immunology;2009-03-24
5. Outcome in patients with Wiskott?Aldrich syndrome following stem cell transplantation: an analysis of 57 patients in Japan;British Journal of Haematology;2006-11
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