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366 related items for PubMed ID: 19388932
21. A founder mutation in the MPL gene causes congenital amegakaryocytic thrombocytopenia (CAMT) in the Ashkenazi Jewish population. Jalas C, Anderson SL, Laufer T, Martimucci K, Bulanov A, Xie X, Ekstein J, Rubin BY. Blood Cells Mol Dis; 2011 Jun 15; 47(1):79-83. PubMed ID: 21489838 [Abstract] [Full Text] [Related]
24. Implications of mutations in hematopoietic growth factor receptor genes in congenital cytopenias. Germeshausen M, Ballmaier M, Welte K. Ann N Y Acad Sci; 2001 Jun 15; 938():305-20; discussion 320-1. PubMed ID: 11458519 [Abstract] [Full Text] [Related]
28. Severe Clinical Course in a Patient with Congenital Amegakaryocytic Thrombocytopenia Due to a Missense Mutation of the c-MPL Gene. Ok Bozkaya İ, Yaralı N, Işık P, Ünsal Saç R, Tavil B, Tunç B. Turk J Haematol; 2015 Jun 15; 32(2):172-4. PubMed ID: 26316487 [Abstract] [Full Text] [Related]
29. Genomic and computational analysis of four novel variants of MPL gene in Congenital Amegakaryocytic Thrombocytopenia. Shah A, Kumar C, Shanmukhaiah C, Rajendran A, Mudaliar S, Idicula-Thomas S, Vundinti BR. Ann Hematol; 2023 Oct 15; 102(10):2683-2693. PubMed ID: 37438490 [Abstract] [Full Text] [Related]
33. Congenital amegakaryocytic thrombocytopenia with multiple physical anomalies in a female neonate. Saqlain N, Ahmed N, Qamar U. J Coll Physicians Surg Pak; 2014 Nov 15; 24 Suppl 3():S253-5. PubMed ID: 25518793 [Abstract] [Full Text] [Related]
34. CAMT in a female with developmental delay, facial malformations and central nervous system anomalies. Martinón-Torres N, Vázquez-Donsión M, Loidi L, Couselo JM. Pediatr Blood Cancer; 2011 Mar 15; 56(3):452-3. PubMed ID: 21225925 [Abstract] [Full Text] [Related]
36. Case Report: Clinical Variation in Children With Thrombopoietin Receptor (C-MPL) Mutations: Report of 2 Cases. Lo C, Alvarez E, Ohgami RS, Jeng M. J Pediatr Hematol Oncol; 2018 Jan 15; 40(1):67-70. PubMed ID: 28859041 [Abstract] [Full Text] [Related]