These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
146 related articles for article (PubMed ID: 1356960)
1. Biology of inherited coagulopathies: factor IX. Larson PJ; High KA Hematol Oncol Clin North Am; 1992 Oct; 6(5):999-1009. PubMed ID: 1356960 [TBL] [Abstract][Full Text] [Related]
2. [Gene mutation and gene diagnosis of hemophilia]. Kojima T Nihon Seirigaku Zasshi; 1998; 60(1):31-42. PubMed ID: 9614303 [No Abstract] [Full Text] [Related]
3. A factor IX gene probe: its use in carrier detection, antenatal diagnosis and characterisation of the molecular basis for hemophilia B. Trent RJ; Svirklys L; Power PA; Rickard KA; Lammi A; Kronenberg H Aust N Z J Med; 1985 Dec; 15(6):721-6. PubMed ID: 3869438 [TBL] [Abstract][Full Text] [Related]
4. Diagnosis of hemophilia B carriers using two novel dinucleotide polymorphisms and Hha I RFLP of the factor IX gene in Japanese subjects. Toyozumi H; Kojima T; Matsushita T; Hamaguchi M; Tanimoto M; Saito H Thromb Haemost; 1995 Oct; 74(4):1009-14. PubMed ID: 8560402 [TBL] [Abstract][Full Text] [Related]
5. Detection of carrier status of hemophilia B using DNA markers. Ishak R; Zakaria Z Southeast Asian J Trop Med Public Health; 1997 Sep; 28(3):629-30. PubMed ID: 9561621 [TBL] [Abstract][Full Text] [Related]
6. Hemophilia B carrier determination based on family-specific mutation detection by DNA single-strand conformation analysis. Poon MC; Anand S; Fraser BM; Hoar DI; Sinclair GD J Lab Clin Med; 1993 Jul; 122(1):55-63. PubMed ID: 8320491 [TBL] [Abstract][Full Text] [Related]
7. [Structure and function of factor VIII and factor IX gene and molecular DNA diagnosis in hemophilia A and B]. Herrmann FH; Wehnert M; Wulff K Z Arztl Fortbild (Jena); 1988; 82(22):1116-22. PubMed ID: 2907834 [No Abstract] [Full Text] [Related]
8. 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]
9. New FACTOR IX linked marker alleles in African Haemophilia B patients. Mitchell C; Mitchell CL; Krause A Haemophilia; 2007 Sep; 13(5):642-4. PubMed ID: 17880456 [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. Molecular basis of hemophilia. Lozier JN; High KA Hematol Pathol; 1990; 4(1):1-26. PubMed ID: 2111315 [No Abstract] [Full Text] [Related]
12. Haemophilia management: the application of DNA analysis for prenatal diagnosis. Van de Water NS; Ockelford PA; Berry EW; Browett PJ N Z Med J; 1991 Oct; 104(922):443-6. PubMed ID: 1681487 [TBL] [Abstract][Full Text] [Related]
13. Structure and function of factor IX: defects in haemophilia B. McGraw RA; Davis LM; Lundblad RL; Stafford DW; Roberts HR Clin Haematol; 1985 Jun; 14(2):359-83. PubMed ID: 3899439 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Molecular analysis and genetic diagnosis of hemophilia. b. Hemophilia B]. Kojima T Nihon Rinsho; 1987 Dec; 45(12):2941-6. PubMed ID: 2895820 [No Abstract] [Full Text] [Related]
16. 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]
17. Molecular genetics and counselling in haemophilia. Peake I Thromb Haemost; 1995 Jul; 74(1):40-4. PubMed ID: 8578494 [TBL] [Abstract][Full Text] [Related]
18. Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphism. Bröcker-Vriends AH; Briët E; Quadt R; Bertina RM; van der Linden IK; van de Kamp JJ; Pearson PL; Veltkamp JJ Thromb Haemost; 1985 Aug; 54(2):506-9. PubMed ID: 3001965 [TBL] [Abstract][Full Text] [Related]
19. Carrier detection in hemophilia using pedigree analysis coagulation tests and DNA probes. de la Salle C; Baas MJ; Grunebaum L; Wiesel ML; Blanco A; Gialeraki R; Mandalaki T; Cazenave JP Nouv Rev Fr Hematol (1978); 1989; 31(3):193-202. PubMed ID: 2575737 [TBL] [Abstract][Full Text] [Related]
20. From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm. Oberlé I; Mandel JL Horiz Biochem Biophys; 1986; 8():51-89. PubMed ID: 2875934 [No Abstract] [Full Text] [Related] [Next] [New Search]