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3. Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene. Wulff K; Bykowska K; Lopaciuk S; Herrmann FH Acta Biochim Pol; 1999; 46(3):721-6. PubMed ID: 10698280 [TBL] [Abstract][Full Text] [Related]
4. Molecular biology of hemophilia B. Roberts HR Thromb Haemost; 1993 Jul; 70(1):1-9. PubMed ID: 8236083 [No Abstract] [Full Text] [Related]
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6. Identification of a novel large F9 gene mutation-an insertion of an Alu repeated DNA element in exon e of the factor 9 gene. Wulff K; Gazda H; Schröder W; Robicka-Milewska R; Herrmann FH Hum Mutat; 2000 Mar; 15(3):299. PubMed ID: 10679958 [No Abstract] [Full Text] [Related]
7. Why does the mutation G17736A/Val107Val (silent) in the F9 gene cause mild haemophilia B in five Swedish families? Knobe KE; Sjörin E; Ljung RC Haemophilia; 2008 Jul; 14(4):723-8. PubMed ID: 18459950 [TBL] [Abstract][Full Text] [Related]
8. Five novel factor IX mutations in unrelated hemophilia B patients. David D; Moreira I; Morais S; de Deus G Hum Mutat; 1998; Suppl 1():S301-3. PubMed ID: 9452115 [No Abstract] [Full Text] [Related]
9. [Double mutation, a 2-bp deletion and Val211Ile, in the blood coagulation factor IX gene of a patient with severe hemophilia B]. Seita I; Shinozawa K; Otaki M; Fujita S; Suzuki T; Amano K; Inaba H; Fukutake K Rinsho Byori; 2009 May; 57(5):417-24. PubMed ID: 19522246 [TBL] [Abstract][Full Text] [Related]
10. Marker and real-time quantitative analyses to confirm hemophilia B carrier diagnosis of a complete deletion of the F9 gene. Venceslá A; Barceló MJ; Baena M; Quintana M; Baiget M; Tizzano EF Haematologica; 2007 Nov; 92(11):1583-4. PubMed ID: 18024414 [TBL] [Abstract][Full Text] [Related]
11. A novel nonsense mutation in exon 2 of the factor IX gene resulting in severe haemophilia B. Niceta M; Fabiano C; Sammarco P; Gagliano F; Mancuso G Intern Emerg Med; 2006; 1(4):318-20. PubMed ID: 17217158 [No Abstract] [Full Text] [Related]
12. Allelic heterogeneity of molecular events in human coagulation factor IX in Asian Indians. Mutation in brief #965. Online. Mahajan A; Chavali S; Ghosh S; Kabra M; Chowdhury MR; ; Bharadwaj D Hum Mutat; 2007 May; 28(5):526. PubMed ID: 17397055 [TBL] [Abstract][Full Text] [Related]
13. [Four novel point mutations of factor IX gene detected by denaturing gradient gel electrophoresis]. Wang Y; Li Z; Wan H Zhonghua Xue Ye Xue Za Zhi; 1998 Mar; 19(3):125-8. PubMed ID: 11243142 [TBL] [Abstract][Full Text] [Related]
14. Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing. Karimipoor M; Zeinali S; Nafissi N; Tuddenham EG; Lak M; Safaee R Thromb Res; 2007; 120(1):135-9. PubMed ID: 17014892 [TBL] [Abstract][Full Text] [Related]
15. Molecular analyses in hemophilia B families: identification of six new mutations in the factor IX gene. Espinós C; Casaña P; Haya S; Cid AR; Aznar JA Haematologica; 2003 Feb; 88(2):235-6. PubMed ID: 12604421 [No Abstract] [Full Text] [Related]
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20. Mutations associated with hemophilia B in Turkish patients. Cağlayan SH; Gökmen Y; Aktuğlu G; Gürgey A; Sommer SS Hum Mutat; 1997; 10(1):76-9. PubMed ID: 9222764 [No Abstract] [Full Text] [Related] [Next] [New Search]