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 *

78 related articles for article (PubMed ID: 10686501)

  • 1. Prenatal determination of a variable number of tandem repeats in intron 40 of the von Willebrand factor gene from maternal peripheral blood using the polymerase chain reaction.
    Ni X; Guo J; Xia J; Li L
    Hum Hered; 2000; 50(3):201-4. PubMed ID: 10686501
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene.
    Peake IR; Bowen D; Bignell P; Liddell MB; Sadler JE; Standen G; Bloom AL
    Blood; 1990 Aug; 76(3):555-61. PubMed ID: 2378985
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Von Willebrand factor 1 and factor 2 alleles (intron 40) are suitable markers for carrier detection in von Willebrand disease families in the Indian population.
    Trasi S; Mohanty D; Pathare A; Shetty S; Ghosh K
    Acta Haematol; 2006; 115(1-2):64-7. PubMed ID: 16424652
    [TBL] [Abstract][Full Text] [Related]  

  • 4. von Willebrand disease family studies: comparison of three methods of analysis of the von Willebrand factor gene polymorphism related to a variable number tandem repeat sequence in intron 40.
    Gaucher C; Mercier B; Mazurier C
    Br J Haematol; 1992 Sep; 82(1):73-80. PubMed ID: 1419805
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Investigation on VNTR in intron 40 of vWF gene in Chinese Han population].
    Ni X; Guo J; Xia J; Li L
    Yi Chuan Xue Bao; 1996; 23(1):1-10. PubMed ID: 8695174
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Allelic frequencies of three VNTRs in intron 40 of the human von Willebrand factor gene in types 1, 2, and 3 von Willebrand disease patients and controls of a Brazilian population.
    Mazzini J; Hackel C; Annichino-Bizzacchi JM
    Thromb Res; 2000 Dec; 100(6):489-94. PubMed ID: 11152928
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis in severe von Willebrand disease families from India using combination of phenotypic and genotypic assays.
    Kasatkar P; Shetty S; Ghosh K
    Prenat Diagn; 2014 Apr; 34(4):377-81. PubMed ID: 24390653
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Instability of repeats of the von Willebrand factor gene variable number tandem repeat sequence in intron 40.
    Eikenboom JC; Reitsma PH; van der Velden PA; Briët E
    Br J Haematol; 1993 Jul; 84(3):533-5. PubMed ID: 8105872
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Von Willebrand gene tracking by single-tube automated fluorescent analysis of four short tandem repeat polymorphisms.
    Vidal F; Julià A; Altisent C; Puig L; Gallardo D
    Thromb Haemost; 2005 May; 93(5):976-81. PubMed ID: 15886817
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Instability in the ATCT variable number tandem repeat locus VWF.VNTR I in intron 40 of von Willebrand factor gene.
    Haddad AP; Sparrow RL
    Br J Haematol; 1997 Sep; 98(3):662-4. PubMed ID: 9332324
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Von Willebrand factor short sequence repeat locus 2 (intron 40) consists of three polymorphic subloci.
    Othman M; Elbatarny HS; Byrne CD; O'Shaughnessy DF
    Acta Haematol; 2007; 117(3):177-80. PubMed ID: 17159339
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two novel alleles of the ATCT variable number tandem repeat locus VWF.VNTR I in intron 40 of the von Willebrand factor gene.
    Haddad AP; Sparrow RL
    Br J Haematol; 1997 Feb; 96(2):298-300. PubMed ID: 9029016
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex variability of intron 40 of the von Willebrand factor (vWF) gene.
    Hering S; Augustin C; Edelmann J; Heidel M; Chamaon K; Dressler J; Szibor R
    Int J Legal Med; 2008 Jan; 122(1):67-71. PubMed ID: 17273877
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiplex fluorescent PCR for noninvasive prenatal detection of fetal-derived paternally inherited diseases using circulatory fetal DNA in maternal plasma.
    Tang DL; Li Y; Zhou X; Li X; Zheng F
    Eur J Obstet Gynecol Reprod Biol; 2009 May; 144(1):35-9. PubMed ID: 19285775
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-invasive prenatal paternity testing from maternal blood.
    Wagner J; Dzijan S; Marjanović D; Lauc G
    Int J Legal Med; 2009 Jan; 123(1):75-9. PubMed ID: 18949481
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Carrier detection and prenatal diagnosis of hemophilia A.
    Xuefeng W; Yuanfang L; Zhiguang L; Haiyan C; Xiaojie S; Yishi F; Hongli W
    Clin Chem Lab Med; 2001 Dec; 39(12):1204-8. PubMed ID: 11798076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Single and double incompatibility at vWA and D8S1179/D21S11 loci between mother and child: implications in kinship analysis.
    Narkuti V; Vellanki RN; Anubrolu N; Doddapaneni KK; Gandhi Kaza PC; Mangamoori LN
    Clin Chim Acta; 2008 Sep; 395(1-2):162-5. PubMed ID: 18503761
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detection of engraftment and mixed chimerism following bone marrow transplantation using PCR amplification of a highly variable region-variable number of tandem repeats (VNTR) in the von Willebrand factor gene.
    Gaiger A; Mannhalter C; Hinterberger W; Haas O; Marosi C; Kier P; Eichinger S; Funovic M; Lechner K
    Ann Hematol; 1991 Oct; 63(4):227-8. PubMed ID: 1932304
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Amplification of a variable number of tandem repeats (VNTR) locus (pMCT118) by the polymerase chain reaction (PCR) and its application to forensic science.
    Kasai K; Nakamura Y; White R
    J Forensic Sci; 1990 Sep; 35(5):1196-200. PubMed ID: 2230693
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Feasibility study of using fetal DNA in maternal plasma for non-invasive prenatal diagnosis.
    Liu FM; Wang XY; Feng X; Wang W; Ye YX; Chen H
    Acta Obstet Gynecol Scand; 2007; 86(5):535-41. PubMed ID: 17464580
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.