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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 6331274)

  • 1. Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome.
    Boyd Y; Buckle VJ; Munro EA; Choo KH; Migeon BR; Craig IW
    Ann Hum Genet; 1984 May; 48(2):145-52. PubMed ID: 6331274
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.
    Mattei MG; Baeteman MA; Heilig R; Oberlé I; Davies K; Mandel JL; Mattei JF
    Hum Genet; 1985; 69(4):327-31. PubMed ID: 2985491
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.
    Schwartz C; Fitch N; Phelan MC; Richer CL; Stevenson R
    Hum Genet; 1987 May; 76(1):54-7. PubMed ID: 3471705
    [TBL] [Abstract][Full Text] [Related]  

  • 4. More precise localization of the human factor IX gene by in situ hybridization.
    Quirk S; Chou WG; Polakowska R; Zain SB; Young FE; Doherty RA
    Cytogenet Cell Genet; 1985; 39(2):121-4. PubMed ID: 3839179
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).
    Camerino G; Grzeschik KH; Jaye M; De La Salle H; Tolstoshev P; Lecocq JP; Heilig R; Mandel JL
    Proc Natl Acad Sci U S A; 1984 Jan; 81(2):498-502. PubMed ID: 6320191
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome.
    Kling S; Coffey AJ; Ljung R; Sjörin E; Nilsson IM; Holmberg L; Giannelli F
    Eur J Haematol; 1991 Oct; 47(4):257-61. PubMed ID: 1683292
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Repeated DNA sequences in the distal long arm of the human X chromosome.
    Müller U; Tantravahi U; Monaco A; Stroh H; Kunkel LM; Latt SA
    Hum Genet; 1986 Sep; 74(1):24-9. PubMed ID: 3019869
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Physical mapping of the factor VIII gene proximal to two polymorphic DNA probes in human chromosome band Xq28: implications for factor VIII gene segregation analysis.
    Tantravahi U; Murty VV; Jhanwar SC; Toole JJ; Woozney JM; Chaganti RS; Latt SA
    Cytogenet Cell Genet; 1986; 42(1-2):75-9. PubMed ID: 3013509
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nullisomic deletion of the mcf.2 transforming gene in two haemophilia B patients.
    Anson DS; Blake DJ; Winship PR; Birnbaum D; Brownlee GG
    EMBO J; 1988 Sep; 7(9):2795-9. PubMed ID: 2846283
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.
    Oberlé I; Drayna D; Camerino G; White R; Mandel JL
    Proc Natl Acad Sci U S A; 1985 May; 82(9):2824-8. PubMed ID: 2986139
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA analysis of seven patients with hemophilia B who have anti-factor IX antibodies: relationship to clinical manifestations and evidence that the abnormal gene was inherited.
    Tanimoto M; Kojima T; Kamiya T; Takamatsu J; Ogata K; Obata Y; Inagaki M; Iizuka A; Nagao T; Kurachi K
    J Lab Clin Med; 1988 Sep; 112(3):307-13. PubMed ID: 3411192
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Regional localization of the human factor IX gene by molecular hybridization.
    Chance PF; Dyer KA; Kurachi K; Yoshitake S; Ropers HH; Wieacker P; Gartler SM
    Hum Genet; 1983; 65(2):207-8. PubMed ID: 6686210
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hemophilia B with inhibitor: molecular analysis of the subtotal deletion of the factor IX gene.
    Hassan HJ; Leonardi A; Guerriero R; Chelucci C; Cianetti L; Ciavarella N; Ranieri P; Pilolli D; Peschle C
    Blood; 1985 Sep; 66(3):728-30. PubMed ID: 2992643
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Isolation and characterization of human random cDNA clones homologous to DNA from the X chromosome.
    Balazs I; Purrello M; Kurnit DM; Grzeschik KH; Siniscalco M
    Somat Cell Mol Genet; 1984 Jul; 10(4):385-97. PubMed ID: 6087473
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gene deletion in an Italian haemophilia B subject.
    Bernardi F; del Senno L; Barbieri R; Buzzoni D; Gambari R; Marchetti G; Conconi F; Panicucci F; Positano M; Pitruzzello S
    J Med Genet; 1985 Aug; 22(4):305-7. PubMed ID: 4045960
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22----q24) by somatic cell hybrid analysis and in situ hybridization.
    Barton DE; Yang-Feng TL; Francke U
    Hum Genet; 1986 Mar; 72(3):221-4. PubMed ID: 2870017
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of the factor IX gene as a result of translocation t(X;1) in a girl affected by haemophilia B.
    Krepischi-Santos AC; Carneiro JD; Svartman M; Bendit I; Odone-Filho V; Vianna-Morgante AM
    Br J Haematol; 2001 Jun; 113(3):616-20. PubMed ID: 11380446
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Assignment of the growth hormone gene locus to 19q26-qter in cattle and to 11q25-qter in sheep by in situ hybridization.
    Hediger R; Johnson SE; Barendse W; Drinkwater RD; Moore SS; Hetzel J
    Genomics; 1990 Sep; 8(1):171-4. PubMed ID: 2081592
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MspI polymorphic site within the factor IX gene. Localization of the site and an improved method for detection.
    Freedenberg DL; Chen SH; Kurachi K; Scott CR
    Hum Genet; 1987 Jul; 76(3):262-4. PubMed ID: 2439437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.