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6. Wiskott-Aldrich syndrome is an important differential diagnosis in male infants with juvenile myelomonocytic leukemialike features. Watanabe N, Yoshimi A, Kamachi Y, Kawabe T, Muramatsu H, Matsumoto K, Manabe A, Kojima S, Kato K. J Pediatr Hematol Oncol; 2007 Dec 01; 29(12):836-8. PubMed ID: 18090932 [Abstract] [Full Text] [Related]
11. Microthrombocytopenia in a male infant with cytomegalovirus. Krishnan KR, Vega R. Ann Allergy Asthma Immunol; 2009 Sep 20; 103(3):268-9. PubMed ID: 19788027 [No Abstract] [Full Text] [Related]
12. A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4. Doğu F, Ariga T, Ikincioğullari A, Bozdoğan G, Aytekin C, Metin A, Babacan E. Turk J Pediatr; 2006 Sep 20; 48(1):66-8. PubMed ID: 16562789 [Abstract] [Full Text] [Related]
17. Multiple independent second-site mutations in two siblings with somatic mosaicism for Wiskott-Aldrich syndrome. Boztug K, Germeshausen M, Avedillo Díez I, Gulacsy V, Diestelhorst J, Ballmaier M, Welte K, Maródi L, Chernyshova L, Klein C. Clin Genet; 2008 Jul 20; 74(1):68-74. PubMed ID: 18479478 [Abstract] [Full Text] [Related]
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20. Development of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome. Boztug K, Dewey RA, Klein C. Curr Opin Mol Ther; 2006 Oct 20; 8(5):390-5. PubMed ID: 17078381 [Abstract] [Full Text] [Related] Page: [Next] [New Search]