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.
122 related articles for article (PubMed ID: 11927134)
1. Suitability of four polymorphic DNA markers for indirect genetic diagnosis of haemophilia A in Japanese subject. Sawada A; Sumita C; Higasa S; Ueda M; Suehiro A; Kakishita E Thromb Res; 2002 Feb; 105(3):271-6. PubMed ID: 11927134 [TBL] [Abstract][Full Text] [Related]
2. [Significance of BclI and HindIII polymorphism detection in genetic diagnosis of familial hemophilia A]. Qiao XQ; Li YP; Zeng L; Chen Y; Han X Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2011 Feb; 19(1):189-92. PubMed ID: 21362249 [TBL] [Abstract][Full Text] [Related]
3. Application of Indirect Linkage Analysis for Carrier Detection of Hemophilia A in Kurdistan Region of Iraq: Usefulness of Intron 18 BclI T>A, Intron 19 HindIII C>T, and IVS7 nt27 G>A Markers. Abdulqader AMR; Rachid S; Mohammed AI; Mahmood SN Clin Appl Thromb Hemost; 2019; 25():1076029619854545. PubMed ID: 31179744 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Factor VIII gene haplotypes and linkage disequilibrium for the indirect genetic analysis of hemophilia A in India. Singh M; Singh P Clin Appl Thromb Hemost; 2009; 15(3):334-9. PubMed ID: 18160577 [TBL] [Abstract][Full Text] [Related]
6. Detection of hemophilia a carriers in Azeri Turkish population of Iran: usefulness of HindIII and BclI markers. Moharrami T; Derakhshan SM; Pourfeizi AA; Khaniani MS Clin Appl Thromb Hemost; 2015 Nov; 21(8):755-9. PubMed ID: 24671757 [TBL] [Abstract][Full Text] [Related]
7. 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]
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. Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene. Gitschier J; Drayna D; Tuddenham EG; White RL; Lawn RM Nature; 1985 Apr 25-May 1; 314(6013):738-40. PubMed ID: 2986011 [TBL] [Abstract][Full Text] [Related]
10. A new HindIII restriction fragment length polymorphism in the hemophilia A locus. Ahrens P; Kruse TA; Schwartz M; Rasmussen PB; Din N Hum Genet; 1987 Jun; 76(2):127-8. PubMed ID: 2886419 [TBL] [Abstract][Full Text] [Related]
11. 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]
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. Carrier detection and prenatal diagnosis of hemophilia A in a Korean population by PCR-based analysis of the BclI/intron 18 and St14 VNTR polymorphisms. Choi YM; Hwang D; Choe J; Jun JK; Kim EJ; Moon SY; Cho S J Hum Genet; 2000; 45(4):218-23. PubMed ID: 10944851 [TBL] [Abstract][Full Text] [Related]
14. [A study on the (CA)n in FVIII gene in Han ethnic group in Guangxi Zhuang Autonomous Region by amplification polymorphisms combined with silver staining]. Zhu CJ; Liu JZ; Ou WL; Long GF; Liang Y; Wang ZY; Zheng MC Zhonghua Er Ke Za Zhi; 2007 Jan; 45(1):55-8. PubMed ID: 17349154 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Allele frequencies and molecular diagnosis in haemophilia A and B patients from Russia and from some Asian republics of the former U.S.S.R. Aseev M; Surin V; Baboev K; Gornostaeva N; Kuznetzova T; Kascheeva T; Ivaschenko T; Solovyev G; Mikhailov A; Lebedev V Prenat Diagn; 1994 Jul; 14(7):513-22. PubMed ID: 7971753 [TBL] [Abstract][Full Text] [Related]
19. DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory. Aguilar-Martinez P; Fabre N; Navarro R; Schved JF; Gris JC; Romey MC; Demaille J; Claustres M Genet Couns; 1993; 4(4):311-9. PubMed ID: 7906519 [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]