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 *

388 related articles for article (PubMed ID: 16941728)

  • 21. [Indirect prenatal molecular diagnostic of haemophilia A and B].
    Morales-Machín A; Borjas-Fajardo L; Zabala W; Alvarez F; Fernández E; Zambrano M; Delgado W; Hernández ML; Solis-Añez E; Chacín JA
    Invest Clin; 2008 Sep; 49(3):289-97. PubMed ID: 18846770
    [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. Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.
    Wehnert M; Herrmann FH; Wulff K
    Dis Markers; 1989; 7(2):113-7. PubMed ID: 2567219
    [TBL] [Abstract][Full Text] [Related]  

  • 24. First trimester prenatal diagnosis of haemophilia A using factor VIII gene probe.
    Yoshioka A; Naka H; Nishimura T; Kuze K; Tanaka I; Mikami S; Matsumoto M; Yoshioka K; Fukui H
    Jinrui Idengaku Zasshi; 1989 Jun; 34(2):135-41. PubMed ID: 2570172
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. Inverse shifting PCR based prenatal diagnosis of hemophilia-causative inversions involving int22h and int1h hotspots from chorionic villus samples.
    Radic CP; Rossetti LC; Zuccoli JR; Abelleyro MM; Larripa IB; De Brasi CD
    Prenat Diagn; 2009 Dec; 29(12):1183-5. PubMed ID: 19842127
    [No Abstract]   [Full Text] [Related]  

  • 28. Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders.
    Shetty S; Ghosh K
    Haemophilia; 2007 Mar; 13(2):172-7. PubMed ID: 17286770
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Absence of correlation between X chromosome inactivation pattern and plasma concentration of factor VIII and factor IX in carriers of haemophilia A and B.
    Orstavik KH; Scheibel E; Ingerslev J; Schwartz M
    Thromb Haemost; 2000 Mar; 83(3):433-7. PubMed ID: 10744150
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of new dinucleotide-repeat polymorphisms in factor VIII gene using fluorescent PCR.
    Kim JW; Park SY; Kim YM; Kim JM; Kim DJ; Ryu HM
    Haemophilia; 2005 Jan; 11(1):38-42. PubMed ID: 15660987
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Requiem to prenatal diagnosis of haemophilia A and B using coagulation activity and antigen based assays: not yet!
    Shetty S; Ghosh K; Anbhavne S; Mohanty D
    Eur J Haematol; 2003 Apr; 70(4):253-4. PubMed ID: 12656753
    [No Abstract]   [Full Text] [Related]  

  • 32. [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]  

  • 33. [Genetic diagnosis in haemophiliacs (haemophilia A, B, carrier)].
    Mikami S
    Rinsho Byori; 1990 Jun; Suppl 85():102-13. PubMed ID: 1976834
    [No Abstract]   [Full Text] [Related]  

  • 34. Carrier and prenatal diagnostic strategy and newly identified mutations in Hungarian haemophilia A and B families.
    Bors A; Andrikovics H; Illés Z; Jáger R; Kardos M; Marosi A; Nemes L; Tordai A
    Blood Coagul Fibrinolysis; 2015 Mar; 26(2):161-6. PubMed ID: 25255241
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Analysis of X ba I polymorphism of FVIII gene and its application on prenatal diagnosis for hemophilia A].
    Wang ZY; Liang Y; Zhou Y; Xiao B; Liu JZ
    Zhonghua Xue Ye Xue Za Zhi; 2006 Mar; 27(3):170-2. PubMed ID: 16792918
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Improvement of gene analysis method in hemophilia A and its application of prenatal diagnosis].
    Liang Y; Zhao Y; Wang ZY; Yan M; Xiao B; Liu JZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):437-9. PubMed ID: 17680537
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A modified I-PCR to detect the factor VIII Inv22 for genetic diagnosis and prenatal diagnosis in haemophilia A.
    He ZH; Chen SF; Chen J; Jiang WY
    Haemophilia; 2012 May; 18(3):452-6. PubMed ID: 21992753
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian population.
    Mukundan P; Shetty S; Kulkarni B; Ghosh K
    Prenat Diagn; 2008 Oct; 28(10):920-2. PubMed ID: 18702107
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A.
    Venceslá A; Baena M; Fares Taie L; Cornet M; Baiget M; Tizzano EF
    Haemophilia; 2008 May; 14(3):489-93. PubMed ID: 18384354
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Genetic questions of hemophilia].
    Weissbach G; Lenk H
    Z Gesamte Inn Med; 1981 Jun; 36(11):363-70. PubMed ID: 6795839
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.