214 related articles for article (PubMed ID: 11877059)
1. [Carrier detection and prenatal diagnosis for hemophilia A].
Wang X; Liu Y; Li Z; Chu H; Sang X; Fan Q; Wang H
Zhonghua Xue Ye Xue Za Zhi; 2001 Mar; 22(3):117-20. PubMed ID: 11877059
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [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]
4. Carrier detection and prenatal diagnosis of hemophilia Alpha.
Liu Y; Wang X; Chu H; Li Z; Wang H; Wang Z
Chin Med J (Engl); 2002 Jul; 115(7):991-4. PubMed ID: 12150727
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. 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]
7. [Prenatal diagnosis for fetus with hemophilia A].
Zhao Y; Liang Y; Wang ZY; Xiao B
Zhonghua Fu Chan Ke Za Zhi; 2008 Apr; 43(4):262-5. PubMed ID: 18843965
[TBL] [Abstract][Full Text] [Related]
8. 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]
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. [Detection of factor VIII intron 1 inversion in severe haemophilia A].
Liang Y; Yan ZY; Yan M; Hua BL; Xiao B; Zhao YQ; Liu JZ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):323-5. PubMed ID: 19504449
[TBL] [Abstract][Full Text] [Related]
11. [Application study on inversion diagnosis of F8 gene in hemophilia A].
Qi LY; Jin CL; Lin CK; Ren MH; Dong WH; Sun KL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):405-8. PubMed ID: 17680530
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [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]
14. [Application studies on the gene diagnosis and carrier detection of hemophilia A by using polymerase chain reaction-conformation sensitive gel electrophoresis].
Lillicrap D; He GP; Leggo J; Liu YS; Tong XH; Zhou GX; Luo LH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):393-9. PubMed ID: 20017302
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. 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]
18. Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia A.
Andrikovics H; Klein I; Bors A; Nemes L; Marosi A; Váradi A; Tordai A
Haematologica; 2003 Jul; 88(7):778-84. PubMed ID: 12857556
[TBL] [Abstract][Full Text] [Related]
19. Prevalence of the factor 8 gene intron 1 inversion in Chinese haemophiliacs and its application to carrier detection and prenatal diagnosis in haemophilia A families.
Lu YL; Wang XF; Ding QL; Dai J; Xi XD; Wang HL
Haemophilia; 2011 May; 17(3):541-2. PubMed ID: 21118339
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
