178 related articles for article (PubMed ID: 19262239)
1. 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]
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. 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]
4. A common G10430A mutation (Gly 60 Ser) in the factor IX gene describes the presence of moderate and mild hemophilia B in the majority of the Gujarati population.
Quadros L; Ghosh K; Shetty S
Ann Hematol; 2007 May; 86(5):377-9. PubMed ID: 17308903
[TBL] [Abstract][Full Text] [Related]
5. 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]
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. 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. 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]
9. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
10. Detection of ten new mutations by screening the gene encoding factor IX of Danish hemophilia B patients.
Nielsen LR; Scheibel E; Ingerslev J; Schwartz M
Thromb Haemost; 1995 May; 73(5):774-8. PubMed ID: 7482402
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Fast and efficient mutation detection method using multiplex PCR and cycle sequencing--application to haemophilia B.
Costa JM; Ernault P; Vidaud D; Vidaud M; Meyer D; Lavergne JM
Thromb Haemost; 2000 Feb; 83(2):244-7. PubMed ID: 10739381
[TBL] [Abstract][Full Text] [Related]
13. [Molecular diagnosis of inherited coagulation disorders--sequence analysis of hemophilia B patients with anti-factor IX antibodies].
Tanimoto M; Matsushita T; Takamatsu J; Saito H
Rinsho Byori; 1990 Sep; 38(9):1041-6. PubMed ID: 2232265
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Molecular analysis of factor IX gene in an Iranian female with severe hemophilia B.
Karimipoor M; Kokabee L; Kamali E; Karizi SZ; Zeinali S
Acta Haematol; 2008; 119(3):151-3. PubMed ID: 18434706
[TBL] [Abstract][Full Text] [Related]
16. 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 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]
18. 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]
19. 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]
20. The Canadian "National Program for hemophilia mutation testing" database: a ten-year review.
Rydz N; Leggo J; Tinlin S; James P; Lillicrap D
Am J Hematol; 2013 Dec; 88(12):1030-4. PubMed ID: 23913812
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
