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 *

125 related articles for article (PubMed ID: 1810022)

  • 1. Evaluation of DNA-based diagnosis for haemophilia A.
    Wadelius C; Blombäck M; Goonewardena P; Anvret M; Lindstedt M; Gustavson KH; Pettersson U
    Scand J Clin Lab Invest; 1991 Nov; 51(7):625-33. PubMed ID: 1810022
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Carrier detection and prenatal diagnosis in 98 families of haemophilia A by linkage analysis and direct detection of mutations.
    Lavergne JM; Laurian Y; Dudilleux A; Larrieu MJ; Bahnak BR; Meyer D
    Blood Coagul Fibrinolysis; 1991 Apr; 2(2):293-301. PubMed ID: 1680009
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multiplex analysis of two intragenic microsatellite repeat polymorphisms in the genetic diagnosis of haemophilia A.
    Windsor S; Taylor SA; Lillicrap D
    Br J Haematol; 1994 Apr; 86(4):810-5. PubMed ID: 7918077
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Hemophilia A: genetic prediction and linkage studies in all available families in Finland.
    Lehesjoki AE; Sistonen P; Rasi V; de la Chapelle A
    Clin Genet; 1991 Mar; 39(3):199-209. PubMed ID: 2036741
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Determination of haemophilia A carrier status from hair samples using polymerase chain reaction technique.
    Hussain S; Shamim A; Vencer L; Butt AI; al-Harithy R; Nasim A
    Clin Genet; 1994 Sep; 46(3):263-7. PubMed ID: 7820943
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms.
    Moodie P; Liddell MB; Peake IR; Bloom AL
    Br J Haematol; 1988 Sep; 70(1):77-84. PubMed ID: 2902876
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Factor VIII gene polymorphisms in North Indian population: a consensus algorithm for carrier analysis of hemophilia A.
    Srinivasan A; Mukhopadhyay S; Karim Z; Gupta RK; Gupta A; Wadhawan V; Shukla J; Singh VP; Dash D
    Clin Chim Acta; 2002 Nov; 325(1-2):177-81. PubMed ID: 12367784
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of haemophilia A in China.
    Liang Y; Zhao Y; Yan M; Fan XP; Xiao B; Liu JZ
    Prenat Diagn; 2009 Jul; 29(7):664-7. PubMed ID: 19399824
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [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. Genetic diagnosis of haemophilia A of Chinese origin.
    Lin SR; Chang SC; Lee CC; Shen MC; Lin SW
    Br J Haematol; 1995 Nov; 91(3):722-7. PubMed ID: 8555082
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular biological approaches to genetic disorders in prenatal diagnosis.
    Katayama S
    Early Hum Dev; 1992; 29(1-3):149-53. PubMed ID: 1356752
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of haemophilia A.
    Chan V; Tong TM; Chan TP; Tang M; Wan CW; Chan FY; Chu YC; Chan TK
    Br J Haematol; 1989 Dec; 73(4):497-500. PubMed ID: 2575402
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Analysis of Factor VIII polymorphic markers as a means for carrier detection in Brazilian families with haemophilia A.
    de Carvalho FM; de Vargas Wolfgramm E; Paneto GG; de Paula Careta F; Spagnol Perrone AM; de Paula F; Louro ID
    Haemophilia; 2007 Jul; 13(4):409-12. PubMed ID: 17610558
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Haemophilia A: carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphism.
    Tuddenham EG; Goldman E; McGraw A; Kernoff PB
    J Clin Pathol; 1987 Sep; 40(9):971-7. PubMed ID: 2889753
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The prenatal diagnosis of hemophilia A--the use of PCR and family RFLP analysis].
    Bian M
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Apr; 15(2):102-7. PubMed ID: 7902217
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Carrier detection and prenatal diagnosis of hemophilia A.
    Xuefeng W; Yuanfang L; Zhiguang L; Haiyan C; Xiaojie S; Yishi F; Hongli W
    Clin Chem Lab Med; 2001 Dec; 39(12):1204-8. PubMed ID: 11798076
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A.
    Wion KL; Tuddenham EG; Lawn RM
    Nucleic Acids Res; 1986 Jun; 14(11):4535-42. PubMed ID: 3012474
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.