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2. Spectrum of factor IX gene mutations causing haemophilia B from India. Ghosh K; Quadros L; Shetty S Blood Coagul Fibrinolysis; 2009 Jul; 20(5):333-6. PubMed ID: 19357501 [TBL] [Abstract][Full Text] [Related]
3. Clinical significance of two mutations in the factor IX gene in a family with haemophilia B. Sexton A; Furmedge J; Barnes C; Cheetham G; Wallace J; Savarirayan R Haemophilia; 2010 Mar; 16(2):374-6. PubMed ID: 19930472 [No Abstract] [Full Text] [Related]
4. FIX mutation spectrum in haemophilia B patients from Jordan: identification of three novel mutations. Awidi A; Alhattab D; Bsoul N; Magablah A; Mefleh R; Dweiri M; Fauori AS Haemophilia; 2011 Jan; 17(1):162-3. PubMed ID: 20695909 [No Abstract] [Full Text] [Related]
5. Identification of novel and recurrent mutations in Tunisian haemophilia B patients. Elmahmoudi H; Khodjet-El-Khil H; Ben-Amor M; Jlizi A; Zahra K; Meddeb B; Ben-Ammar-El-Gaaied A; Gouider E Haemophilia; 2011 May; 17(3):544-5. PubMed ID: 21118338 [No Abstract] [Full Text] [Related]
6. [Gene diagnosis of 3 haemophilia B families]. Zhang Y; Yang LH; Lu YL; Ding QL; Wang XF; Liu XE; Zhang L Zhonghua Xue Ye Xue Za Zhi; 2008 Mar; 29(3):179-82. PubMed ID: 18788618 [TBL] [Abstract][Full Text] [Related]
7. Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations. Attali O; Vinciguerra C; Trzeciak MC; Durin A; Pernod G; Gay V; Ménart C; Sobas F; Dechavanne M; Négrier C Thromb Haemost; 1999 Nov; 82(5):1437-42. PubMed ID: 10595634 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Mutation analysis of haemophilia B in the Irish population: increased prevalence caused by founder effect. Jenkins PV; Egan H; Keenan C; O'Shea E; Smith OP; Nolan B; White B; O'Donnell J Haemophilia; 2008 Jul; 14(4):717-22. PubMed ID: 18479429 [TBL] [Abstract][Full Text] [Related]
11. Heteroduplex analysis in hemophilia B: detection of two novel factor IX gene mutations. Driscoll MC; Chu A; Hilgartner MW Am J Hematol; 1996 Apr; 51(4):324-7. PubMed ID: 8602635 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Methylation of the factor IX gene--a basic reason for the mutation causing hemophilia B]. Mazin AL Mol Biol (Mosk); 1995; 29(1):71-90. PubMed ID: 7723765 [TBL] [Abstract][Full Text] [Related]
14. Deep intronic mutations are rarely a cause of hemophilia B. Feng J; Liu Q; Drost J; Sommer SS Hum Mutat; 1999; 14(3):267-8. PubMed ID: 10477436 [No Abstract] [Full Text] [Related]
15. Twenty-five novel mutations of the factor IX gene in haemophilia B. Wulff K; Schröder W; Wehnert M; Herrmann FH Hum Mutat; 1995; 6(4):346-8. PubMed ID: 8680410 [No Abstract] [Full Text] [Related]
17. Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India. Jayandharan GR; Shaji RV; Baidya S; Nair SC; Chandy M; Srivastava A Thromb Haemost; 2005 Oct; 94(4):883-6. PubMed ID: 16270648 [No Abstract] [Full Text] [Related]
18. Double mutations in haemophilia: muddling strangers or indifferent partners in crime? Nair PS; Shetty S; Ghosh K Haemophilia; 2010 Nov; 16(6):970-1. PubMed ID: 20546034 [No Abstract] [Full Text] [Related]
19. 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]
20. [A survey of families with hemophilia B in Sweden. Almost all of the examined have unique mutations]. Ljung R Lakartidningen; 1994 Sep; 91(38):3380-2. PubMed ID: 7990572 [No Abstract] [Full Text] [Related] [Next] [New Search]