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7. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia. Andreu N; Matamoros N; Escudero A; Fillat C Int J Mol Med; 2007 May; 19(5):777-82. PubMed ID: 17390083 [TBL] [Abstract][Full Text] [Related]
8. Wiskott-Aldrich syndrome in a Jamaican. Walters JP; Morais P West Indian Med J; 1993 Jun; 42(2):79-81. PubMed ID: 8367970 [TBL] [Abstract][Full Text] [Related]
9. A rare case of Wiskott-Aldrich Syndrome with normal platelet size: a case report. Baharin MF; Dhaliwal JS; Sarachandran SV; Idris SZ; Yeoh SL J Med Case Rep; 2016 Jun; 10(1):188. PubMed ID: 27356510 [TBL] [Abstract][Full Text] [Related]
10. 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; 48(1):66-8. PubMed ID: 16562789 [TBL] [Abstract][Full Text] [Related]
11. [Wiscott-Aldrich syndrome. Description of a case]. Brai M; Balsamo V; Mogavero S; Romano N; Lagrutta A G Batteriol Virol Immunol; 1975; 68(1-6):130-9. PubMed ID: 1081964 [TBL] [Abstract][Full Text] [Related]
12. 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; 74(1):68-74. PubMed ID: 18479478 [TBL] [Abstract][Full Text] [Related]
17. Wiskott-Aldrich syndrome. A case report. Dubiel A; Szczerbinski T; Kurtyka Z; Kowalczyk D Clin Pediatr (Phila); 1990 Aug; 29(8):434-7. PubMed ID: 2208901 [TBL] [Abstract][Full Text] [Related]
18. The usefulness of X-linked polymorphic loci as gene markers to track X allele and chimerism in a post-allogeneic peripheral blood stem cell transplant patient with Wiskott-Aldrich syndrome. Sasanakul W; Hongeng S; Chuansumrit A; Chaiyaratana W; Pakakasama S; Hathirat P J Med Assoc Thai; 2001 Mar; 84(3):379-84. PubMed ID: 11460939 [TBL] [Abstract][Full Text] [Related]
19. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR. Proust A; Guillet B; Picard C; de Saint Basile G; Pondarré C; Tamary H; Dreyfus M; Tchernia G; Fischer A; Delaunay J Blood Cells Mol Dis; 2007; 39(1):102-6. PubMed ID: 17400488 [TBL] [Abstract][Full Text] [Related]
20. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Itoh S; Nonoyama S; Morio T; Imai K; Okawa H; Ochs HD; Shimadzu M; Yata J Int J Hematol; 2000 Jan; 71(1):79-83. PubMed ID: 10729999 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]