141 related articles for article (PubMed ID: 11128113)
1. St 14 (DX S52) VNTR polymorphism in the Indian population and its application in carrier detection and prenatal diagnosis of haemophilia A families.
Shetty S; Ghosh K; Mohanty D
Haematologia (Budap); 2000; 30(3):203-7. PubMed ID: 11128113
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [Diagnosis of hemophilia A by a combination of St14(DXS52) VNTR polymorphism and (CA)n repeat polymorphism within FVIII gene].
Zhong CG; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):80-2. PubMed ID: 14767918
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A.
Gallegos RM; Aranda HB; Navarrete CP; Espinoza R; Gómez FS; Aranda DA
Am J Hematol; 2004 Sep; 77(1):1-6. PubMed ID: 15307098
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Rapid polymerase chain reaction analysis of St14 (DXS52) VNTR: carrier detection of hemophilia A.
Yang YH; Song KS; Kim IK; Cha DH
J Obstet Gynaecol Res; 1997 Aug; 23(4):399-406. PubMed ID: 9311183
[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. 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]
11. 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]
12. [The St14 (DXS 52) VNTR in a Guangdong Han population and detection of hemophilia A carriers].
Ma A; Zeng R; He Q
Zhonghua Xue Ye Xue Za Zhi; 2000 Jul; 21(7):362-5. PubMed ID: 11877006
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. 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]
15. 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]
16. [Diagnosis of hemophilia A carrier state using analysis of intergenic and intergenic polymorphism of factor VIII gene].
Sawecka J; Strzyga P; Klukowska A; Rokicka-Milewska R; Kościelak J
Pol Arch Med Wewn; 1995 Nov; 94(5):425-31. PubMed ID: 8833940
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Improvement of gene analysis method in hemophilia A and its application of prenatal diagnosis].
Liang Y; Zhao Y; Wang ZY; Yan M; Xiao B; Liu JZ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):437-9. PubMed ID: 17680537
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. The value of St14 (DXS52) VNTR analysis for genetic diagnosis of hemophilia A in Iranian population.
Babak Azimifar S; Yoosef Seyedna S; Zeinali S
Thromb Res; 2006; 118(4):505-7. PubMed ID: 16325238
[No Abstract] [Full Text] [Related]
[Next] [New Search]
