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2. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann's thrombasthenia. Bray PF, Shuman MA. Blood; 1990 Feb 15; 75(4):881-8. PubMed ID: 1967954 [Abstract] [Full Text] [Related]
3. The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel. Newman PJ, Seligsohn U, Lyman S, Coller BS. Proc Natl Acad Sci U S A; 1991 Apr 15; 88(8):3160-4. PubMed ID: 2014236 [Abstract] [Full Text] [Related]
4. Truncation of glycoprotein (GP) IIIa (616-762) prevents complex formation with GPIIb: novel mutation in exon 11 of GPIIIa associated with thrombasthenia. Ferrer M, Tao J, Iruín G, Sánchez-Ayuso M, González-Rodríguez J, Parrilla R, González-Manchón C. Blood; 1998 Dec 15; 92(12):4712-20. PubMed ID: 9845537 [Abstract] [Full Text] [Related]
8. [Analysis of the GPIIb and GPIIIa genes in patients with Glanzmann's thrombasthenia]. Yasunaga M, Ryo R, Adachi M, Sugano W, Yoshida A, Nakayama K, Saigo K, Yasunaga K, Yamaguchi N. Rinsho Ketsueki; 1992 Feb 15; 33(2):133-8. PubMed ID: 1635160 [Abstract] [Full Text] [Related]
14. [Molecular pathology of inherited Glanzmann's thrombasthenia. Report of 11 cases]. Ruan CG, Gu JM, Li JY. Zhonghua Nei Ke Za Zhi; 1992 Oct 15; 31(10):639-41, 659. PubMed ID: 1306460 [Abstract] [Full Text] [Related]
15. Ser-752-->Pro mutation in the cytoplasmic domain of integrin beta 3 subunit and defective activation of platelet integrin alpha IIb beta 3 (glycoprotein IIb-IIIa) in a variant of Glanzmann thrombasthenia. Chen YP, Djaffar I, Pidard D, Steiner B, Cieutat AM, Caen JP, Rosa JP. Proc Natl Acad Sci U S A; 1992 Nov 01; 89(21):10169-73. PubMed ID: 1438206 [Abstract] [Full Text] [Related]
19. Platelet vitronectin receptor expression differentiates Iraqi-Jewish from Arab patients with Glanzmann thrombasthenia in Israel. Coller BS, Cheresh DA, Asch E, Seligsohn U. Blood; 1991 Jan 01; 77(1):75-83. PubMed ID: 1702031 [Abstract] [Full Text] [Related]