335 related articles for article (PubMed ID: 17555134)
1. [Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: a new marker for the hemophilia A carrier detection].
Surin VL; Luk'ianenko AV; Luchinina IuA
Genetika; 2007 Apr; 43(4):560-6. PubMed ID: 17555134
[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. 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]
4. [XbaI polymorphism in intron 22 of factor VIII and gene potential for prenatal diagnosis of hemophilia A].
Shen Y
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1990 Aug; 12(4):281-5. PubMed ID: 1979254
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Allele frequencies of three factor VIII gene polymorphisms in Iranian populations and their application in hemophilia A carrier detection.
Azimifar SB; Seyedna SY; Zeinali S
Am J Hematol; 2006 May; 81(5):335-9. PubMed ID: 16628729
[TBL] [Abstract][Full Text] [Related]
7. Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian population.
Mukundan P; Shetty S; Kulkarni B; Ghosh K
Prenat Diagn; 2008 Oct; 28(10):920-2. PubMed ID: 18702107
[TBL] [Abstract][Full Text] [Related]
8. [Analysis of X ba I polymorphism of FVIII gene and its application on prenatal diagnosis for hemophilia A].
Wang ZY; Liang Y; Zhou Y; Xiao B; Liu JZ
Zhonghua Xue Ye Xue Za Zhi; 2006 Mar; 27(3):170-2. PubMed ID: 16792918
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. [Detection of carriers of hemophilia A by testing for HindIII polymorphism in the factor VIII gene by PCR].
Surin VL; Aseev MV; Zhukova EL; Baranov VS; Solov'ev GIa; Grineva NI; Andreeva TA; Izhevskaia VL; Likhacheva EA; Pliushch OP
Genetika; 1990 Oct; 26(10):1840-6. PubMed ID: 2149345
[TBL] [Abstract][Full Text] [Related]
12. [Molecular genetic study of the factor VIII gene in families from Bashkir with hemophilia A].
Sultanaeva ZM; Viktorova TV; Aseev MV; Baranov VS; Khusnutdinova EK
Genetika; 2000 May; 36(5):699-703. PubMed ID: 10867889
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism--Indian experience.
Chowdhury MR; Tiwari M; Kabra M; Menon PS
Ann Hematol; 2003 Jul; 82(7):427-30. PubMed ID: 12768323
[TBL] [Abstract][Full Text] [Related]
19. Hemophilia A. Detection of molecular defects and of carriers by DNA analysis.
Antonarakis SE; Waber PG; Kittur SD; Patel AS; Kazazian HH; Mellis MA; Counts RB; Stamatoyannopoulos G; Bowie EJ; Fass DN
N Engl J Med; 1985 Oct; 313(14):842-8. PubMed ID: 2993888
[TBL] [Abstract][Full Text] [Related]
20. [Assessment of the frequency of finding polymorphic alleles of the human X-chromosome locus DXS52 in the Muscovite population].
Kaĭdalova AI; Smirnova OV; Surin VL; Solov'ev GIa
Genetika; 1994 Jul; 30(7):966-8. PubMed ID: 7958812
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]