173 related articles for article (PubMed ID: 15307098)
1. 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]
2. 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]
3. 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]
4. [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]
5. Carrier detection of hemophilia A in a Mexican population by two Bcl I polymorphisms.
Carrillo Pérez MD; Fragoso Herrera R; Cisneros Vega B; Amparo Esparza M; Cantú JM; Montañez Ojeda C
Arch Med Res; 1993; 24(2):139-42. PubMed ID: 7903882
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Polymorphism distribution of ST14(DXS52) VNTR in normal individuals in northeastern region of China and its application in gene diagnosis of hemophilia A].
Chunlian J; Changkun L; Jun S; Li J; Wenhan D; Xue Z; Kailai S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Feb; 15(1):31-4. PubMed ID: 9456369
[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. 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]
10. [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]
11. Allele frequencies of two polymorphisms associated with the factor IX gene in Iranian population.
Ghandil P; Ghadiri A; Farhud D; Zeinali S
Thromb Res; 2004; 113(5):289-93. PubMed ID: 15183040
[TBL] [Abstract][Full Text] [Related]
12. Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe.
Oberle I; Camerino G; Heilig R; Grunebaum L; Cazenave JP; Crapanzano C; Mannucci PM; Mandel JL
N Engl J Med; 1985 Mar; 312(11):682-6. PubMed ID: 2983207
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Molecular detection or carriers of hemophilia A in Mexican families.
Rojas-Martínez A; Villalobos-Torres MC; Ortiz-de-Luna RI; Pompa-Garza MT; Barrera-Saldaña HA
Rev Invest Clin; 1996; 48(2):125-7. PubMed ID: 8815496
[TBL] [Abstract][Full Text] [Related]
16. A rapid multifluorescent polymerase chain reaction for genetic counselling in Chinese haemophilia A families.
Fang Y; Wang XF; Dai J; Wang HL
Haemophilia; 2006 Jan; 12(1):62-7. PubMed ID: 16409177
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]