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 *

185 related articles for article (PubMed ID: 6421151)

  • 21. Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.
    Filippi G; Rinaldi A; Palmarino R; Seravalli E; Siniscalco M
    Genetics; 1977 May; 86(1):199-212. PubMed ID: 301840
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis of haemophilia.
    Ljung RC
    Baillieres Clin Haematol; 1996 Jun; 9(2):243-57. PubMed ID: 8800503
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Mutation screening of the F VIII gene in 10 hemophilia A families].
    LI W; HU X; GAO BD; LI LY; LIAO Y; TANG XM; TANG WL; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):127-32. PubMed ID: 21462120
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Inversion of intron 22 in isolated cases of severe hemophilia A.
    Tizzano EF; Domènech M; Baiget M
    Thromb Haemost; 1995 Jan; 73(1):6-9. PubMed ID: 7740498
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Carrier detection of ovine hemophilia A using an RFLP marker, and mapping of the factor VIII gene on the ovine X-chromosome.
    Backfisch W; Neuenschwander S; Giger U; Stranzinger G; Pliska V
    J Hered; 1994; 85(6):474-8. PubMed ID: 7995928
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Factor VIII gene inversions and polymorphisms in Brazilian patients with haemophilia A: carrier detection and prenatal diagnosis.
    Soares RP; Chamone DA; Bydlowski SP
    Haemophilia; 2001 May; 7(3):299-305. PubMed ID: 11380635
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Color blindness not closely linked to bipolar illness. Report of a new pedigree series.
    Gershon ES; Targum SD; Matthysse S; Bunney WE
    Arch Gen Psychiatry; 1979 Dec; 36(13):1423-30. PubMed ID: 316315
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Application of Indirect Linkage Analysis for Carrier Detection of Hemophilia A in Kurdistan Region of Iraq: Usefulness of Intron 18 BclI T>A, Intron 19 HindIII C>T, and IVS7 nt27 G>A Markers.
    Abdulqader AMR; Rachid S; Mohammed AI; Mahmood SN
    Clin Appl Thromb Hemost; 2019; 25():1076029619854545. PubMed ID: 31179744
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis by linkage: hemophilia A and polymorphic glucose-6-phosphate deydrogenase.
    Edgell CJ; Kirkman HN; Clemons E; Buchanan PD; Miller CH
    Am J Hum Genet; 1978 Jan; 30(1):80-4. PubMed ID: 623105
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic counseling of hemophilia carriers.
    Ljung R; Tedgård U
    Semin Thromb Hemost; 2003 Feb; 29(1):31-6. PubMed ID: 12640562
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Screening of intron 1 inversion and three intragenic factor VIII gene polymorphisms in Pakistani hemophilia A families.
    Bugvi SM; Imran M; Mahmood S; Hafeez R; Fatima W; Sohail S
    Blood Coagul Fibrinolysis; 2012 Mar; 23(2):132-7. PubMed ID: 22270795
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular genetics of hemophilia A.
    Gitschier J
    Schweiz Med Wochenschr; 1989 Sep; 119(39):1329-31. PubMed ID: 2508218
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Interaction of incontinentia pigmenti and factor VIII mutations in a female with biased X inactivation, resulting in haemophilia.
    Coleman R; Genet SA; Harper JI; Wilkie AO
    J Med Genet; 1993 Jun; 30(6):497-500. PubMed ID: 8326493
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Factor VIII gene inversions in severe hemophilia A patients.
    Van de Water NS; Williams R; Nelson J; Browett PJ
    Pathology; 1995 Jan; 27(1):83-5. PubMed ID: 7603762
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A.
    Bicocchi MP; Migeon BR; Pasino M; Lanza T; Bottini F; Boeri E; Molinari AC; Corsolini F; Morerio C; Acquila M
    Eur J Hum Genet; 2005 May; 13(5):635-40. PubMed ID: 15741993
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hemophilia A. Detection of molecular defects and of carriers by DNA analysis.
    Antonarakis SE; Waber PG; Kittur SD; Patel AS; Kazazian HH; Mellis MA; Counts RB; Stamatoyannopoulos G; Bowie EJ; Fass DN
    N Engl J Med; 1985 Oct; 313(14):842-8. PubMed ID: 2993888
    [TBL] [Abstract][Full Text] [Related]  

  • 37. High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.
    Citron M; Godmilow L; Ganguly T; Ganguly A
    Hum Mutat; 2002 Oct; 20(4):267-74. PubMed ID: 12325022
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular analysis of hemophilia A mutations in the Finnish population.
    Levinson B; Lehesjoki AE; de la Chapelle A; Gitschier J
    Am J Hum Genet; 1990 Jan; 46(1):53-62. PubMed ID: 2104741
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A.
    Sampietro M; Camerino G; Romano M; Cappellini MD; Fiorelli G; Brambati B; Guerneri S; Ferrari M; Travi M; Krachmalnicoff A
    Thromb Haemost; 1987 Dec; 58(4):988-92. PubMed ID: 3127923
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hemophilia A: role of FVIIIC/vWF Ag in assisting linkage analysis for carrier detection.
    Ahmed RP; Gupta PK; Kannan M; Suresh K; Kashyap R; Choudhry VP; Saxena R
    Clin Appl Thromb Hemost; 2004 Apr; 10(2):127-31. PubMed ID: 15094932
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.