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 *

163 related articles for article (PubMed ID: 15750001)

  • 21. Carrier detection by DNA linkage analysis in eighty Thai hemophilia A families.
    Mahasandana C; Pung-Amritt P; Treesucon A; Petrarat S; Veerakul G; Visudhiphan S; Yenchitsomanus PT
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S513-21. PubMed ID: 12403227
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2.
    Kakourou G; Dhanjal S; Daphnis D; Doshi A; Nuttall S; Gotts S; Serhal P; Delhanty J; Harper J; SenGupta S
    Prenat Diagn; 2007 Feb; 27(2):111-6. PubMed ID: 17192963
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A.
    Gallegos RM; Aranda HB; Navarrete CP; Espinoza R; Gómez FS; Aranda DA
    Am J Hematol; 2004 Sep; 77(1):1-6. PubMed ID: 15307098
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Preimplantation genetic diagnosis: state of the art.
    Basille C; Frydman R; El Aly A; Hesters L; Fanchin R; Tachdjian G; Steffann J; LeLorc'h M; Achour-Frydman N
    Eur J Obstet Gynecol Reprod Biol; 2009 Jul; 145(1):9-13. PubMed ID: 19411132
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Multiplex fluorescent analysis of four short tandem repeats for rapid haemophilia A molecular diagnosis.
    Sánchez-García JF; Gallardo D; Ramírez L; Vidal F
    Thromb Haemost; 2005 Nov; 94(5):1099-103. PubMed ID: 16363255
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Preimplantation genetic diagnosis for BRCA1 exon 13 duplication mutation using linked polymorphic markers resulting in a live birth.
    Jasper MJ; Liebelt J; Hussey ND
    Prenat Diagn; 2008 Apr; 28(4):292-8. PubMed ID: 18302307
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Preimplantation genetic diagnosis for neurofibromatosis type 1.
    Spits C; De Rycke M; Van Ranst N; Joris H; Verpoest W; Lissens W; Devroey P; Van Steirteghem A; Liebaers I; Sermon K
    Mol Hum Reprod; 2005 May; 11(5):381-7. PubMed ID: 15833774
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?
    Reches A; Malcov M; Ben-Yosef D; Azem F; Amit A; Yaron Y
    Prenat Diagn; 2009 Jan; 29(1):57-61. PubMed ID: 19097038
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1.
    Altarescu G; Brooks B; Kaplan Y; Eldar-Geva T; Margalioth EJ; Levy-Lahad E; Renbaum P
    Hum Reprod; 2006 Aug; 21(8):2047-51. PubMed ID: 16740526
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A successful strategy for Preimplantation Genetic Diagnosis of beta-thalassemia and simultaneous detection of Down's syndrome using multiplex fluorescent PCR.
    Piyamongkol W; Vutyavanich T; Piyamongkol S; Wells D; Kunaviktikul C; Tongsong T; Chaovisitsaree S; Saetung R; Sanguansermsri T
    J Med Assoc Thai; 2006 Jul; 89(7):918-27. PubMed ID: 16881421
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Case report: first successful application of preimplantation genetic diagnosis for hereditary angiooedema.
    Bautista-Llácer R; Alberola TM; Vendrell X; Fernández E; Pérez-Alonso M
    Reprod Biomed Online; 2010 Nov; 21(5):658-62. PubMed ID: 20888297
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplification.
    Ren Z; Zeng HT; Xu YW; Zhuang GL; Deng J; Zhang C; Zhou CQ
    Fertil Steril; 2009 Feb; 91(2):359-64. PubMed ID: 18359022
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Genetic diagnosis of polycystic kidney disease using single cell fluorescent polymerase chain reaction].
    Huang J; Liu P; Chen YJ; Zhang H; Zheng DX; Zhang XW; Qiao J
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2007 Apr; 29(2):283-6. PubMed ID: 17536286
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Carrier detection and prenatal diagnosis of hemophilia in developing countries.
    Peyvandi F
    Semin Thromb Hemost; 2005 Nov; 31(5):544-54. PubMed ID: 16276463
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families.
    Hussein IR; El-Beshlawy A; Salem A; Mosaad R; Zaghloul N; Ragab L; Fayek H; Gaber K; El-Ekiabi M
    Haemophilia; 2008 Sep; 14(5):1082-7. PubMed ID: 18547262
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The value of St14 (DXS52) VNTR analysis for genetic diagnosis of hemophilia A in Iranian population.
    Babak Azimifar S; Yoosef Seyedna S; Zeinali S
    Thromb Res; 2006; 118(4):505-7. PubMed ID: 16325238
    [No Abstract]   [Full Text] [Related]  

  • 39. Carrier detection and prenatal diagnosis of hemophilia Alpha.
    Liu Y; Wang X; Chu H; Li Z; Wang H; Wang Z
    Chin Med J (Engl); 2002 Jul; 115(7):991-4. PubMed ID: 12150727
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Preimplantation genetic diagnosis for hemophilia A using indirect linkage analysis and direct genotyping approaches.
    Laurie AD; Hill AM; Harraway JR; Fellowes AP; Phillipson GT; Benny PS; Smith MP; George PM
    J Thromb Haemost; 2010 Apr; 8(4):783-9. PubMed ID: 20102489
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.