164 related articles for article (PubMed ID: 7913672)
21. Carrier detection by direct gene analysis in a family with haemophilia B (factor IX deficiency).
Peake IR; Furlong BL; Bloom AL
Lancet; 1984 Feb; 1(8371):242-3. PubMed ID: 6142993
[TBL] [Abstract][Full Text] [Related]
22. Carrier detection for hemophilia B: evaluation of multiple polymorphic sites.
Mariani G; Chistolini A; Hassan HJ; Gallo E; Gu XG; Papacchini M; Di Paolantonio T; Fantoni A
Am J Hematol; 1990 Jan; 33(1):1-7. PubMed ID: 1967154
[TBL] [Abstract][Full Text] [Related]
23. A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia B.
Montandon AJ; Green PM; Bentley DR; Ljung R; Nilsson IM; Giannelli F
Curr Stud Hematol Blood Transfus; 1991; (58):88-93. PubMed ID: 1954781
[No Abstract] [Full Text] [Related]
24. 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]
25. Screening for mutations in the gene encoding factor IX.
Nielsen LR; Schwartz M; Scheibel E
J Inherit Metab Dis; 1992; 15(3):339-41. PubMed ID: 1357229
[No Abstract] [Full Text] [Related]
26. [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]
27. Use of factor IX intragenic recombinant DNA probes for evaluation of carrier status in haemophilia B families of Irish origin.
Geraghty M; Sarsfield P; Temperley I; Humphries P
Ir J Med Sci; 1986 Dec; 155(12):419-24. PubMed ID: 3818253
[No Abstract] [Full Text] [Related]
28. 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]
29. Comparison of phenotypic assessment and the use of two restriction fragment length polymorphisms in the diagnosis of the carrier state in haemophilia B.
Lillicrap DP; Liddell MB; Matthews RJ; Peake IR; Bloom AL
Br J Haematol; 1986 Mar; 62(3):557-65. PubMed ID: 3006741
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis of haemophilia.
Ljung RC
Baillieres Clin Haematol; 1996 Jun; 9(2):243-57. PubMed ID: 8800503
[TBL] [Abstract][Full Text] [Related]
31. A rapid method for haemophilia B mutation detection using conformation sensitive gel electrophoresis.
Hinks JL; Winship PR; Makris M; Preston FE; Peake IR; Goodeve AC
Br J Haematol; 1999 Mar; 104(4):915-8. PubMed ID: 10192459
[TBL] [Abstract][Full Text] [Related]
32. The Malmö polymorphism of factor IX: establishing the genotypes by rapid analysis of DNA.
Graham JB; Kunkel GR; Tennyson GS; Lord ST; Fowlkes DM
Blood; 1989 Jun; 73(8):2104-7. PubMed ID: 2567187
[TBL] [Abstract][Full Text] [Related]
33. Heteroduplex screening for molecular defects in factor IX genes from haemophilia B families.
Chen SH; Schoof JM; Weinmann AF; Thompson AR
Br J Haematol; 1995 Feb; 89(2):409-12. PubMed ID: 7873393
[TBL] [Abstract][Full Text] [Related]
34. Allele frequencies of two polymorphisms associated with the factor IX gene in Iranian population.
Ghandil P; Ghadiri A; Farhud D; Zeinali S
Thromb Res; 2004; 113(5):289-93. PubMed ID: 15183040
[TBL] [Abstract][Full Text] [Related]
35. Single nucleotide primer extension to detect genetic diseases: experimental application to hemophilia B (factor IX) and cystic fibrosis genes.
Kuppuswamy MN; Hoffmann JW; Kasper CK; Spitzer SG; Groce SL; Bajaj SP
Proc Natl Acad Sci U S A; 1991 Feb; 88(4):1143-7. PubMed ID: 1671714
[TBL] [Abstract][Full Text] [Related]
36. Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland.
Connor JM; Pettigrew AF; Hann IM; Forbes CD; Lowe GD; Affara NA
J Med Genet; 1985 Dec; 22(6):441-6. PubMed ID: 4078877
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. Female twins with severe Christmas disease (hemophilia B).
Wollina K; Bowen DJ; Syrbe G; Zintl F
Thromb Haemost; 1993 Nov; 70(5):774-6. PubMed ID: 7907444
[TBL] [Abstract][Full Text] [Related]
40. Carrier testing in hemophilia B with an immunoassay that distinguishes a prevalent factor IX dimorphism.
Smith KJ; Thompson AR; McMullen BA; Frazier D; Lin SW; Stafford D; Kisiel W; Thibodeau SN; Chen SH; Smith LF
Blood; 1987 Oct; 70(4):1006-13. PubMed ID: 3651597
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]