These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

338 related articles for article (PubMed ID: 25255241)

  • 1. Carrier and prenatal diagnostic strategy and newly identified mutations in Hungarian haemophilia A and B families.
    Bors A; Andrikovics H; Illés Z; Jáger R; Kardos M; Marosi A; Nemes L; Tordai A
    Blood Coagul Fibrinolysis; 2015 Mar; 26(2):161-6. PubMed ID: 25255241
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The status of carrier and prenatal diagnosis of haemophilia in China.
    Dai J; Lu Y; Ding Q; Wang H; Xi X; Wang X
    Haemophilia; 2012 Mar; 18(2):235-40. PubMed ID: 21910785
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 104(922):443-6. PubMed ID: 1681487
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. New FACTOR IX linked marker alleles in African Haemophilia B patients.
    Mitchell C; Mitchell CL; Krause A
    Haemophilia; 2007 Sep; 13(5):642-4. PubMed ID: 17880456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Genomic diagnosis of haemophilia A and B in the German Democratic Republic.
    Herrmann FH; Wehnert M; Schröder W
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1990; 117(4):601-7. PubMed ID: 1714866
    [TBL] [Abstract][Full Text] [Related]  

  • 10. First-trimester prenatal diagnosis in haemophilia A and B families--10 years experience from a centre in India.
    Shetty S; Ghosh K; Jijina F
    Prenat Diagn; 2006 Nov; 26(11):1015-7. PubMed ID: 16941728
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. [Intragenic polymorphisms of factor VIII and IX genes and their utility in the indirect diagnosis of carriers of Haemophilias A and B].
    Borjas L; Zabala W; Pineda L; Pardo T; Fernández E; Zambrano M; Quintero JM; Arteaga-Vizcaíno M; Morales-Machín A; Delgado W
    Invest Clin; 2010 Sep; 51(3):391-401. PubMed ID: 21305775
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 57(2):131-6. PubMed ID: 2885943
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 75(5):424-8. PubMed ID: 1982946
    [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. A haemophilia A and B molecular genetic diagnostic programme in Hungary: a highly informative and cost-effective strategy.
    Klein I; Andrikovics H; Bors A; Nemes L; Tordai A; Váradi A
    Haemophilia; 2001 May; 7(3):306-12. PubMed ID: 11380636
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of haemophilia: a preliminary report.
    Shetty S; Colah R; Gorakshakar A; Bhide A; Ghosh K; Pathare A; Jijina F; Mohanty D
    Natl Med J India; 1998; 11(5):218-9. PubMed ID: 10997168
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. 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]  

    [Next]    [New Search]
    of 17.