BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 11798076)

  • 1. 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]  

  • 2. [Carrier detection and prenatal diagnosis for hemophilia A].
    Wang X; Liu Y; Li Z; Chu H; Sang X; Fan Q; Wang H
    Zhonghua Xue Ye Xue Za Zhi; 2001 Mar; 22(3):117-20. PubMed ID: 11877059
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Informativeness of linkage analysis for genetic diagnosis of haemophilia A in India.
    Jayandharan G; Shaji RV; George B; Chandy M; Srivastava A
    Haemophilia; 2004 Sep; 10(5):553-9. PubMed ID: 15357783
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [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]  

  • 7. [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]  

  • 8. 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]  

  • 9. [Prenatal diagnosis for fetus with hemophilia A].
    Zhao Y; Liang Y; Wang ZY; Xiao B
    Zhonghua Fu Chan Ke Za Zhi; 2008 Apr; 43(4):262-5. PubMed ID: 18843965
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. High-resolution combined linkage physical map of short tandem repeat loci on human chromosome band Xq28 for indirect haemophilia A carrier detection.
    Machado FB; Medina-Acosta E
    Haemophilia; 2009 Jan; 15(1):297-308. PubMed ID: 18752533
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Carrier detection and prenatal diagnosis in families with haemophilia.
    Shetty S; Ghosh K; Bhide A; Mohanty D
    Natl Med J India; 2001; 14(2):81-3. PubMed ID: 11396323
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. [Detection of factor VIII intron 1 inversion in severe haemophilia A].
    Liang Y; Yan ZY; Yan M; Hua BL; Xiao B; Zhao YQ; Liu JZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):323-5. PubMed ID: 19504449
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Diagnosis of hemophilia A carrier state using analysis of intergenic and intergenic polymorphism of factor VIII gene].
    Sawecka J; Strzyga P; Klukowska A; Rokicka-Milewska R; Kościelak J
    Pol Arch Med Wewn; 1995 Nov; 94(5):425-31. PubMed ID: 8833940
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Analysing two dinucleotide repeats of FVIII gene in Iranian population.
    Rabbani B; Rezaeian A; Khanahmad H; Bagheri R; Kamali E; Zeinali S
    Haemophilia; 2007 Nov; 13(6):740-4. PubMed ID: 17973851
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDR.
    Herrmann FH; Kruse T; Wehnert M; Vogel G; Wulff K
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1988; 115(4):489-93. PubMed ID: 2465959
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.