255 related articles for article (PubMed ID: 15086324)
1. Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients.
Mukherjee S; Mukhopadhyay A; Banerjee D; Chandak GR; Ray K
Haemophilia; 2004 May; 10(3):259-63. PubMed ID: 15086324
[TBL] [Abstract][Full Text] [Related]
2. Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.
Mahajan A; Chavali S; Kabra M; Chowdhury MR; Bharadwaj D
Haematologica; 2004 Dec; 89(12):1498-503. PubMed ID: 15590401
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B.
Kwon MJ; Yoo KY; Kim HJ; Kim SH
Haemophilia; 2008 Sep; 14(5):1069-75. PubMed ID: 18624698
[TBL] [Abstract][Full Text] [Related]
6. Molecular genotyping of the Italian cohort of patients with hemophilia B.
Belvini D; Salviato R; Radossi P; Pierobon F; Mori P; Castaldo G; Tagariello G;
Haematologica; 2005 May; 90(5):635-42. PubMed ID: 15921378
[TBL] [Abstract][Full Text] [Related]
7. Six novel and three recurrent mutations in nine Austrian patients with hemophilia B.
Walter J; Pabinger-Fasching I; Watzke HH
Thromb Haemost; 1994 Jul; 72(1):74-7. PubMed ID: 7974379
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Genetic basis and carrier detection of hemophilia B of Chinese origin.
Lin SW; Shen MC
Thromb Haemost; 1993 Mar; 69(3):247-52. PubMed ID: 8470048
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Five novel point mutations: two causing haemophilia B and three causing factor X deficiency.
Odom MW; Leone G; De Stefano V; Montiel MM; Boland EJ; Anderson J; Jagadeeswaran P
Mol Cell Probes; 1994 Feb; 8(1):63-5. PubMed ID: 8028609
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B.
Bicocchi MP; Pasino M; Rosano C; Molinari AC; Della Valle E; Lanza T; Bottini F; Acquila M
Haemophilia; 2006 May; 12(3):263-70. PubMed ID: 16643212
[TBL] [Abstract][Full Text] [Related]
16. Novel human pathological mutations. Gene symbol: F9. Disease: Haemophilia B.
Niazi G; Shaukat Z; Masood K; Hussain R
Hum Genet; 2009 Aug; 126(2):332. PubMed ID: 19693996
[No Abstract] [Full Text] [Related]
17. Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.
Jayandharan G; Shaji RV; Baidya S; Nair SC; Chandy M; Srivastava A
Haemophilia; 2005 Sep; 11(5):481-91. PubMed ID: 16128892
[TBL] [Abstract][Full Text] [Related]
18. Novel mutations in factor IX gene from western India with reference to their phenotypic and haplotypic attributes.
Quadros L; Ghosh K; Shetty S
J Pediatr Hematol Oncol; 2009 Mar; 31(3):157-60. PubMed ID: 19262239
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Factor IX mutations in haemophilia B patients in Malaysia: a preliminary study.
Balraj P; Ahmad M; Khoo AS; Ayob Y
Malays J Pathol; 2012 Jun; 34(1):67-9. PubMed ID: 22870602
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
