BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

469 related articles for article (PubMed ID: 17680530)

  • 41. Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A.
    Bogdanova N; Markoff A; Pollmann H; Nowak-Göttl U; Eisert R; Wermes C; Todorova A; Eigel A; Dworniczak B; Horst J
    Hum Mutat; 2005 Sep; 26(3):249-54. PubMed ID: 16086318
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular genotyping of hemophilia A in Saudi Arabia: report of 2 novel mutations.
    Owaidah TM; Alkhail HA; Zahrani HA; Musa AA; Saleh MA; Riash MA; Alodaib A; Abu Amero K
    Blood Coagul Fibrinolysis; 2009 Sep; 20(6):415-8. PubMed ID: 19448530
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism--Indian experience.
    Chowdhury MR; Tiwari M; Kabra M; Menon PS
    Ann Hematol; 2003 Jul; 82(7):427-30. PubMed ID: 12768323
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Long distance-PCR for detection of factor VIII gene inversion in patients with severe hemophilia A].
    Ding PF; Sun WS; Wang QY; Liu DC; Zhang XQ; Teng B; Shen FK
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2003 Aug; 11(4):390-2. PubMed ID: 12962569
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [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]  

  • 46. The Canadian "National Program for hemophilia mutation testing" database: a ten-year review.
    Rydz N; Leggo J; Tinlin S; James P; Lillicrap D
    Am J Hematol; 2013 Dec; 88(12):1030-4. PubMed ID: 23913812
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Analysis of intron 1 factor VIII gene inversion for direct diagnosis in patients with severe haemophilia A in China.
    Liang Y; Yan M; Xiao B; Liu J
    Prenat Diagn; 2008 Feb; 28(2):160-1. PubMed ID: 18196603
    [No Abstract]   [Full Text] [Related]  

  • 48. Mutation reports: intron 1 and 22 inversions in Indian haemophilics.
    Ahmed R; Kannan M; Choudhry VP; Saxena R
    Ann Hematol; 2003 Sep; 82(9):546-7. PubMed ID: 12879284
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Inversion of intron 1 of the factor VIII gene for direct molecular diagnosis of hemophilia A.
    Tizzano EF; Cornet M; Baiget M
    Haematologica; 2003 Jan; 88(1):118-20. PubMed ID: 12551839
    [No Abstract]   [Full Text] [Related]  

  • 50. Mutational spectrum of F8 gene and prothrombotic gene variants in haemophilia A patients from Southern Italy.
    Sanna V; Zarrilli F; Nardiello P; D'Argenio V; Rocino A; Coppola A; DI Minno G; Castaldo G
    Haemophilia; 2008 Jul; 14(4):796-803. PubMed ID: 18459951
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A rapid multifluorescent polymerase chain reaction for genetic counselling in Chinese haemophilia A families.
    Fang Y; Wang XF; Dai J; Wang HL
    Haemophilia; 2006 Jan; 12(1):62-7. PubMed ID: 16409177
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: a new marker for the hemophilia A carrier detection].
    Surin VL; Luk'ianenko AV; Luchinina IuA
    Genetika; 2007 Apr; 43(4):560-6. PubMed ID: 17555134
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Frequency of intron 1 and 22 inversions of Factor VIII gene in Mexican patients with severe hemophilia A.
    Mantilla-Capacho JM; Beltrán-Miranda CP; Luna-Záizar H; Aguilar-López L; Esparza-Flores MA; López-Guido B; Troyo-Sanromán R; Jaloma-Cruz AR
    Am J Hematol; 2007 Apr; 82(4):283-7. PubMed ID: 17211847
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation.
    Djambas Khayat C; Salem N; Chouery E; Corbani S; Moix I; Nicolas E; Morris MA; de Moerloose P; Mégarbané A
    Haemophilia; 2008 Jul; 14(4):709-16. PubMed ID: 18479430
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Carrier detection and prenatal diagnosis of hemophilia A in a Korean population by PCR-based analysis of the BclI/intron 18 and St14 VNTR polymorphisms.
    Choi YM; Hwang D; Choe J; Jun JK; Kim EJ; Moon SY; Cho S
    J Hum Genet; 2000; 45(4):218-23. PubMed ID: 10944851
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Carrier analysis and prenatal diagnosis of haemophilia A in North India.
    Pandey GS; Phadke SR; Mittal B
    Int J Mol Med; 2002 Nov; 10(5):661-4. PubMed ID: 12373312
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. [XbaI polymorphism in intron 22 of factor VIII and gene potential for prenatal diagnosis of hemophilia A].
    Shen Y
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1990 Aug; 12(4):281-5. PubMed ID: 1979254
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Spectrum of factor VIII mutations in Arab patients with severe haemophilia A.
    Abu-Amero KK; Hellani A; Al-Mahed M; Al-Sheikh I
    Haemophilia; 2008 May; 14(3):484-8. PubMed ID: 18371166
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Detection of intron 22 inversion of factor VIII gene in severe hemophilia A patients].
    Guo ZP; Chen JF; Qin XY; Zhang YF; Yang LH
    Zhonghua Xue Ye Xue Za Zhi; 2013 Nov; 34(11):918-21. PubMed ID: 24294844
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 24.