267 related articles for article (PubMed ID: 10944851)
1. 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]
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. 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]
4. 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]
5. 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]
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. 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]
8. 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]
9. [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]
10. Carrier detection for prenatal diagnosis of hemophilia A in Italian families.
Cappello N; Restagno G; Garnerone S; Gennaro C; Perugini L; Rendine S; Piazza A; Carbonara A
Haematologica; 1992; 77(4):302-6. PubMed ID: 1358771
[TBL] [Abstract][Full Text] [Related]
11. The prevalence study on restriction fragment length polymorphism analysis for the detection of hemophilia A carrier.
Song KS; Lee CH; Chung CS; Lee K; Yang YH; Kim KY
Yonsei Med J; 1993 Sep; 34(3):239-42. PubMed ID: 7903130
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [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]
14. [Restriction fragment length polymorphisms in FVIII:C gene and their application in the linkage analysis of hemophilia A].
He XP; Du CS; Zeng RP; An YH; Liu LL
Yi Chuan Xue Bao; 1991; 18(5):394-400. PubMed ID: 1685886
[TBL] [Abstract][Full Text] [Related]
15. [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]
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. DNA polymorphisms for carrier detection of hemophilia in Thailand.
Chuansumrit A; Goodeve A; Sasanakul W; Peake IR; Pintadit P; Hathirat P; Preston FE; Isarangkul P
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():201-6. PubMed ID: 8629107
[TBL] [Abstract][Full Text] [Related]
18. Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.
Tasleem Raza S; Husain N; Kumar A
Clin Appl Thromb Hemost; 2009 Feb; 15(1):78-83. PubMed ID: 19150994
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]