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Journal Abstract Search

330 related items for PubMed ID: 15183040

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. 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]

  • 23.
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  • 24. [Screening for carrier state of Haemophilia B using indirect genomic detection].
    Kecskés M, Nagy A, Vidra T, Kispál G, Radványi G, Vezendi K, Hajnal L, Kellner R, Losonczy H.
    Orv Hetil; 2001 Feb 18; 142(7):341-4. PubMed ID: 11243016
    [Abstract] [Full Text] [Related]

  • 25.
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  • 26. Haemophilia management: the application of DNA analysis for prenatal diagnosis.
    Van de Water NS, Ockelford PA, Berry EW, Browett PJ.
    N Z Med J; 1991 Oct 23; 104(922):443-6. PubMed ID: 1681487
    [Abstract] [Full Text] [Related]

  • 27. Molecular genetics and counselling in haemophilia.
    Peake I.
    Thromb Haemost; 1995 Jul 23; 74(1):40-4. PubMed ID: 8578494
    [Abstract] [Full Text] [Related]

  • 28. 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 Jul 23; 75(5):424-8. PubMed ID: 1982946
    [Abstract] [Full Text] [Related]

  • 29. Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.
    Connor JM, Pettigrew AF, Shiach C, Hann IM, Lowe GD, Forbes CD.
    J Med Genet; 1986 Aug 23; 23(4):300-9. PubMed ID: 3018248
    [Abstract] [Full Text] [Related]

  • 30. Factor VIII gene mutations and RFLP analysis in hemophilia A.
    Krepelová A, Brdicka R, Vorlová Z.
    Stem Cells; 1993 May 23; 11 Suppl 1():72-6. PubMed ID: 8100465
    [Abstract] [Full Text] [Related]

  • 31. 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 23; 28(10):920-2. PubMed ID: 18702107
    [Abstract] [Full Text] [Related]

  • 32.
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  • 33. [Gene diagnosis of 3 haemophilia B families].
    Zhang Y, Yang LH, Lu YL, Ding QL, Wang XF, Liu XE, Zhang L.
    Zhonghua Xue Ye Xue Za Zhi; 2008 Mar 23; 29(3):179-82. PubMed ID: 18788618
    [Abstract] [Full Text] [Related]

  • 34. Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing.
    Karimipoor M, Zeinali S, Nafissi N, Tuddenham EG, Lak M, Safaee R.
    Thromb Res; 2007 Mar 23; 120(1):135-9. PubMed ID: 17014892
    [Abstract] [Full Text] [Related]

  • 35. 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 Mar 23; 77(4):302-6. PubMed ID: 1358771
    [Abstract] [Full Text] [Related]

  • 36.
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  • 37. Carrier detection of hemophilia A in a Mexican population by two Bcl I polymorphisms.
    Carrillo Pérez MD, Fragoso Herrera R, Cisneros Vega B, Amparo Esparza M, Cantú JM, Montañez Ojeda C.
    Arch Med Res; 1993 Mar 23; 24(2):139-42. PubMed ID: 7903882
    [Abstract] [Full Text] [Related]

  • 38. 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 23; 13(6):740-4. PubMed ID: 17973851
    [Abstract] [Full Text] [Related]

  • 39. [A PCR-system of analyzing polymorphic markers in gamma-A and gamma-G globin genes and gene for human blood coagulation factor IX with an internal control of the completeness of restriction hydrolysis].
    Luk'ianenko AV, Surin VL, Voskoboeva EIu, Tagiev AF, Krutov AA, Solov'ev GIa.
    Genetika; 1993 Mar 23; 29(3):388-92. PubMed ID: 8098004
    [Abstract] [Full Text] [Related]

  • 40. RFLPs of factor IX gene in Japanese haemophilia B families and gene deletion in two high-responder-inhibitor patients.
    Mikami S, Nishino M, Nishimura T, Fukui H.
    Jinrui Idengaku Zasshi; 1987 Mar 23; 32(1):21-31. PubMed ID: 2886685
    [No Abstract] [Full Text] [Related]

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