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.
252 related articles for article (PubMed ID: 7918077)
1. 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]
2. Intragenic dinucleotide repeats in factor VIII gene for the diagnosis of haemophilia A. Yip B; Chan V; Chan TK Br J Haematol; 1994 Dec; 88(4):889-91. PubMed ID: 7819115 [TBL] [Abstract][Full Text] [Related]
3. Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene. Lalloz MR; Schwaab R; McVey JH; Michaelides K; Tuddenham EG Br J Haematol; 1994 Apr; 86(4):804-9. PubMed ID: 7918076 [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. Haemophilia A diagnosis by automated fluorescent DNA detection of ten factor VIII intron 13 dinucleotide repeat alleles. Kochhan L; Lalloz MR; Oldenburg J; McVey JH; Olek K; Brackmann HH; Tuddenham EG; Schwaab R Blood Coagul Fibrinolysis; 1994 Aug; 5(4):497-501. PubMed ID: 7841304 [TBL] [Abstract][Full Text] [Related]
6. 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 [TBL] [Abstract][Full Text] [Related]
7. Factor VIII gene inversions and polymorphisms in Brazilian patients with haemophilia A: carrier detection and prenatal diagnosis. Soares RP; Chamone DA; Bydlowski SP Haemophilia; 2001 May; 7(3):299-305. PubMed ID: 11380635 [TBL] [Abstract][Full Text] [Related]
8. Analysis of the two microsatellite repeat polymorphisms of the factor VIII gene in the Turkish population. Jarjanazi H; Timur AA; El-Maarri O; Cağlayan SH Br J Haematol; 1998 Mar; 100(3):589-93. PubMed ID: 9504646 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene. Lalloz MR; McVey JH; Pattinson JK; Tuddenham EG Lancet; 1991 Jul; 338(8761):207-11. PubMed ID: 1676778 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Factor VIII gene polymorphisms in the Asian Indian population. Chowdhury MR; Herrmann FH; Schroder W; Lambert CT; Lalloz MR; Layton M; Kumbnani HK; Kabra M; Menon PS; Verma IC Haemophilia; 2000 Nov; 6(6):625-30. PubMed ID: 11122386 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. [Hemophilia A: analysis of intron 18 and intron 7 of factor VIII gene and their role in a diagnostic strategy for carrier detection in a Chilean population]. Quiroga T; Goycoolea M; Kaltwasser G; Morales M; Vildósola J; Muñoz B; Pereira J; Mezzano D Rev Med Chil; 1996 Jul; 124(7):777-84. PubMed ID: 9138364 [TBL] [Abstract][Full Text] [Related]
19. Detection of hemophilia A carriers using intragenic factor VIII:C DNA polymorphisms. Janco RL; Phillips JA; Orlando PJ; Woodard MJ; Wion KL; Lawn RM Blood; 1987 May; 69(5):1539-41. PubMed ID: 2882794 [TBL] [Abstract][Full Text] [Related]
20. Screening of intron 1 inversion and three intragenic factor VIII gene polymorphisms in Pakistani hemophilia A families. Bugvi SM; Imran M; Mahmood S; Hafeez R; Fatima W; Sohail S Blood Coagul Fibrinolysis; 2012 Mar; 23(2):132-7. PubMed ID: 22270795 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]