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 *

304 related articles for article (PubMed ID: 1681487)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

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

  • 5. Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphism.
    Bröcker-Vriends AH; Briët E; Quadt R; Bertina RM; van der Linden IK; van de Kamp JJ; Pearson PL; Veltkamp JJ
    Thromb Haemost; 1985 Aug; 54(2):506-9. PubMed ID: 3001965
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [Prenatal diagnosis of hemophilia A by DNA analysis].
    Wu G
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Dec; 13(6):428-34. PubMed ID: 1686577
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [Gene mutation and gene diagnosis of hemophilia].
    Kojima T
    Nihon Seirigaku Zasshi; 1998; 60(1):31-42. PubMed ID: 9614303
    [No Abstract]   [Full Text] [Related]  

  • 12. 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; 77(4):302-6. PubMed ID: 1358771
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnosis of carriers of haemophilia A by RFLP analysis: Austrian results.
    Mannhalter C; Neidhart R; Lechner K
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1990; 117(4):609-15. PubMed ID: 1714867
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A.
    Sampietro M; Camerino G; Romano M; Cappellini MD; Fiorelli G; Brambati B; Guerneri S; Ferrari M; Travi M; Krachmalnicoff A
    Thromb Haemost; 1987 Dec; 58(4):988-92. PubMed ID: 3127923
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.
    Kogan SC; Doherty M; Gitschier J
    N Engl J Med; 1987 Oct; 317(16):985-90. PubMed ID: 3657865
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. DNA polymorphisms for carrier detection of hemophilia in Thailand.
    Chuansumrit A; Goodeve A; Sasanakul W; Peake IR; Pintadit P; Hathirat P; Preston FE; Isarangkul P
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():201-6. PubMed ID: 8629107
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.