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Journal Abstract Search

116 related items for PubMed ID: 19624762

  • 1. Improved criterion-referenced assessment in indirect tracking of haemophilia A using a 0.23 cM-resolution dense polymorphic marker set.
    Machado FB, Duarte LP, Medina-Acosta E.
    Haemophilia; 2009 Sep; 15(5):1135-42. PubMed ID: 19624762
    [Abstract] [Full Text] [Related]

  • 2. Informativeness of a novel multiallelic marker-set comprising an F8 intron 21 and three tightly linked loci for haemophilia A carriership analysis.
    Machado FB, Alves Da Silva AF, Rossetti LC, De Brasi CD, Medina-Acosta E.
    Haemophilia; 2011 Mar; 17(2):257-66. PubMed ID: 21070487
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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]

  • 6. 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]

  • 7. 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]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Indirect carrier detection of canine haemophilia A using factor VIII microsatellite markers.
    Brooks MB, MacNguyen R, Hall R, Gupta R, Booth JG.
    Anim Genet; 2008 Jun; 39(3):278-83. PubMed ID: 18454805
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. 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 May; 4(4):311-9. PubMed ID: 7906519
    [Abstract] [Full Text] [Related]

  • 13. Single-tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A.
    Zhao M, Chen M, Tan ASC, Cheah FSH, Mathew J, Wong PC, Chong SS.
    J Thromb Haemost; 2017 Jul; 15(7):1473-1483. PubMed ID: 28345288
    [Abstract] [Full Text] [Related]

  • 14. Analysis of five polymorphic DNA markers for indirect genetic diagnosis of haemophilia A in the Brazilian population.
    Massaro JD, Wiezel CE, Muniz YC, Rego EM, de Oliveira LC, Mendes-Junior CT, Simões AL.
    Haemophilia; 2011 Sep; 17(5):e936-43. PubMed ID: 21649803
    [Abstract] [Full Text] [Related]

  • 15. Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis.
    Tizzano E, Venceslá A, Cornet M, Baena M, Baiget M.
    Haemophilia; 2005 Mar; 11(2):142-4. PubMed ID: 15810916
    [Abstract] [Full Text] [Related]

  • 16. Interlocus non-random association of multiallelic polymorphisms spanning the coagulation factor VIII gene on human chromosome distalmost Xq28.
    Medina-Acosta E.
    Haemophilia; 2010 May; 16(3):525-37. PubMed ID: 20050928
    [Abstract] [Full Text] [Related]

  • 17. Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian population.
    Mukundan P, Shetty S, Kulkarni B, Ghosh K.
    Prenat Diagn; 2008 Oct; 28(10):920-2. PubMed ID: 18702107
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism--Indian experience.
    Chowdhury MR, Tiwari M, Kabra M, Menon PS.
    Ann Hematol; 2003 Jul 07; 82(7):427-30. PubMed ID: 12768323
    [Abstract] [Full Text] [Related]

  • 20. Analysis of 168 short tandem repeat loci in the Japanese population, using a screening set for human genetic mapping.
    Mizutani M, Yamamoto T, Torii K, Kawase H, Yoshimoto T, Uchihi R, Tanaka M, Tamaki K, Katsumata Y.
    J Hum Genet; 2001 Jul 07; 46(8):448-55. PubMed ID: 11501942
    [Abstract] [Full Text] [Related]

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