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Fechtner syndrome: physiologic analysis of macrothrombocytopenia.
McBane RD, Elliott MA, White JG, Charlesworth JE, Costopoulos MG, Owen WG, Nichols WL. McBane RD, et al. Among authors: white jg. Blood Coagul Fibrinolysis. 2000 Apr;11(3):243-7. Blood Coagul Fibrinolysis. 2000. PMID: 10870804
A novel hereditary macrothrombocytopenia.
Gilman AL, Sloand E, White JG, Sacher R. Gilman AL, et al. Among authors: white jg. J Pediatr Hematol Oncol. 1995 Nov;17(4):296-305. doi: 10.1097/00043426-199511000-00004. J Pediatr Hematol Oncol. 1995. PMID: 7583384
Sebastian syndrome: case report and review of the literature.
Young G, Luban NL, White JG. Young G, et al. Among authors: white jg. Am J Hematol. 1999 May;61(1):62-5. doi: 10.1002/(sici)1096-8652(199905)61:1<62::aid-ajh11>3.0.co;2-a. Am J Hematol. 1999. PMID: 10331513 Free article. Review.
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
Heath KE, Campos-Barros A, Toren A, Rozenfeld-Granot G, Carlsson LE, Savige J, Denison JC, Gregory MC, White JG, Barker DF, Greinacher A, Epstein CJ, Glucksman MJ, Martignetti JA. Heath KE, et al. Among authors: white jg. Am J Hum Genet. 2001 Nov;69(5):1033-45. doi: 10.1086/324267. Epub 2001 Oct 4. Am J Hum Genet. 2001. PMID: 11590545 Free PMC article.
775 results