170 related articles for article (PubMed ID: 2883108)
1. A DNA marker closely linked to the factor IX (haemophilia B) gene.
Mulligan L; Holden JJ; White BN
Hum Genet; 1987 Apr; 75(4):381-3. PubMed ID: 2883108
[TBL] [Abstract][Full Text] [Related]
2. Extragenic factor IX gene RFLP is useful for detecting carriers of Japanese hemophilia B.
Tanimoto M; Kojima T; Ogata K; Hamaguchi M; Takamatsu J; Kamiya T; Saito H
Nihon Ketsueki Gakkai Zasshi; 1989 Jul; 52(4):774-7. PubMed ID: 2575831
[TBL] [Abstract][Full Text] [Related]
3. Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.
Connor JM; Pettigrew AF; Shiach C; Hann IM; Lowe GD; Forbes CD
J Med Genet; 1986 Aug; 23(4):300-9. PubMed ID: 3018248
[TBL] [Abstract][Full Text] [Related]
4. Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms.
Moodie P; Liddell MB; Peake IR; Bloom AL
Br J Haematol; 1988 Sep; 70(1):77-84. PubMed ID: 2902876
[TBL] [Abstract][Full Text] [Related]
5. An MseI RFLP in the 5' flanking region of the factor IX gene: its use for haemophilia B carrier detection in Caucasian and Thai populations.
Winship PR; Nichols CE; Chuansumrit A; Peake IR
Br J Haematol; 1993 May; 84(1):101-5. PubMed ID: 8101718
[TBL] [Abstract][Full Text] [Related]
6. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.
Brown WT; Ye W; Gross AC; Chan CB; Dobkin CS; Jenkins EC
Am J Med Genet; 1988; 30(1-2):551-66. PubMed ID: 2902796
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications.
Forster-Gibson CJ; Mulligan LM; Partington MW; Simpson NE; Holden JJ; White BN
J Neurogenet; 1985 Jun; 2(3):231-7. PubMed ID: 3860635
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers.
Winship PR; Rees DJ; Alkan M
Lancet; 1989 Mar; 1(8639):631-4. PubMed ID: 2564457
[TBL] [Abstract][Full Text] [Related]
11. Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.
Arveiler B; Oberlé I; Vincent A; Hofker MH; Pearson PL; Mandel JL
Am J Hum Genet; 1988 Feb; 42(2):380-9. PubMed ID: 2893549
[TBL] [Abstract][Full Text] [Related]
12. Carrier detection and prenatal diagnosis in families with haemophilia.
Shetty S; Ghosh K; Bhide A; Mohanty D
Natl Med J India; 2001; 14(2):81-3. PubMed ID: 11396323
[TBL] [Abstract][Full Text] [Related]
13. Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).
Giannelli F; Anson DS; Choo KH; Rees DJ; Winship PR; Ferrari N; Rizza CR; Brownlee GG
Lancet; 1984 Feb; 1(8371):239-41. PubMed ID: 6142992
[TBL] [Abstract][Full Text] [Related]
14. Diagnostic role of an immunoassay-detected polymorphism of factor IX for potential carriers of hemophilia B.
Thompson AR; Chen SH; Smith KJ
Blood; 1988 Nov; 72(5):1633-8. PubMed ID: 2902887
[TBL] [Abstract][Full Text] [Related]
15. Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms.
Winship PR; Anson DS; Rizza CR; Brownlee GG
Nucleic Acids Res; 1984 Dec; 12(23):8861-72. PubMed ID: 6096810
[TBL] [Abstract][Full Text] [Related]
16. A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and Western European populations.
Goodeve AC; Chuansumrit A; Sasanakul W; Isarangkura P; Preston FE; Peake IR
Blood Coagul Fibrinolysis; 1994 Feb; 5(1):29-35. PubMed ID: 7910050
[TBL] [Abstract][Full Text] [Related]
17. Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).
Mulley J; Turner G; Bain S; Sutherland GR
Am J Med Genet; 1988; 30(1-2):567-80. PubMed ID: 2902797
[TBL] [Abstract][Full Text] [Related]
18. Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in Polynesians.
Van-de-Water NS; Ridgway D; Ockelford PA
J Med Genet; 1991 Mar; 28(3):171-6. PubMed ID: 1675686
[TBL] [Abstract][Full Text] [Related]
19. Genomic diagnosis of haemophilia A and B in the German Democratic Republic.
Herrmann FH; Wehnert M; Schröder W
Folia Haematol Int Mag Klin Morphol Blutforsch; 1990; 117(4):601-7. PubMed ID: 1714866
[TBL] [Abstract][Full Text] [Related]
20. Factor IX gene haplotypes and its relevance for the indirect genetic analysis of haemophilia B in its Indian perspective.
Singh M; Singh P
Blood Coagul Fibrinolysis; 2008 Jul; 19(5):429-32. PubMed ID: 18600094
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]