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Journal Abstract Search

431 related items for PubMed ID: 18547262

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

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

  • 4. 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 Jan; 45(4):218-23. PubMed ID: 10944851
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  • 5. DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory.
    Aguilar-Martinez P, Fabre N, Navarro R, Schved JF, Gris JC, Romey MC, Demaille J, Claustres M.
    Genet Couns; 1993 Jan; 4(4):311-9. PubMed ID: 7906519
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Carrier detection for prenatal diagnosis of hemophilia A in Italian families.
    Cappello N, Restagno G, Garnerone S, Gennaro C, Perugini L, Rendine S, Piazza A, Carbonara A.
    Haematologica; 1992 Jan; 77(4):302-6. PubMed ID: 1358771
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  • 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. 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
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  • 13. Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphisms.
    Bröcker-Vriends AH, Briët E, Quadt R, Dreesen JC, Bakker E, Claassen-Tegelaar R, Kanhai HH, van de Kamp JJ, Pearson PL.
    Thromb Haemost; 1987 Apr 07; 57(2):131-6. PubMed ID: 2885943
    [Abstract] [Full Text] [Related]

  • 14. 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 07; 77(1):1-6. PubMed ID: 15307098
    [Abstract] [Full Text] [Related]

  • 15. 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 07; 14(3):489-93. PubMed ID: 18384354
    [Abstract] [Full Text] [Related]

  • 16. Carrier detection and prenatal diagnosis in haemophilia A and B.
    Chistolini A, Papacchini M, Mazzucconi MG, La Verde G, Arcieri R, Ferrari A, Paesano R, Pachi A, Mariani G.
    Haematologica; 1990 May 07; 75(5):424-8. PubMed ID: 1982946
    [Abstract] [Full Text] [Related]

  • 17. [Diagnosis of hemophilia A by a combination of St14(DXS52) VNTR polymorphism and (CA)n repeat polymorphism within FVIII gene].
    Zhong CG, Li LY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb 07; 21(1):80-2. PubMed ID: 14767918
    [Abstract] [Full Text] [Related]

  • 18. New FACTOR IX linked marker alleles in African Haemophilia B patients.
    Mitchell C, Mitchell CL, Krause A.
    Haemophilia; 2007 Sep 07; 13(5):642-4. PubMed ID: 17880456
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