169 related articles for article (PubMed ID: 2149345)
21. 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]
22. Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.
Wehnert M; Herrmann FH; Wulff K
Dis Markers; 1989; 7(2):113-7. PubMed ID: 2567219
[TBL] [Abstract][Full Text] [Related]
23. Identification of carriers of haemophilia by polymerase chain reaction.
Winter PC; Butler EE
Ulster Med J; 1993 Apr; 62(1):21-8. PubMed ID: 8100097
[TBL] [Abstract][Full Text] [Related]
24. Molecular genetics and counselling in haemophilia.
Peake I
Thromb Haemost; 1995 Jul; 74(1):40-4. PubMed ID: 8578494
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. [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]
27. 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]
28. 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]
29. [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]
30. 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]
31. Simple and convenient detection of a HindIII polymorphic site in intron 19 of factor VIII using PCR.
Surin VL; Zhukova EL; Krutov AA; Solovyev GYa ; Grineva NI
Nucleic Acids Res; 1990 Jun; 18(11):3432. PubMed ID: 1972572
[No Abstract] [Full Text] [Related]
32. Carrier detection in hemophilia using pedigree analysis coagulation tests and DNA probes.
de la Salle C; Baas MJ; Grunebaum L; Wiesel ML; Blanco A; Gialeraki R; Mandalaki T; Cazenave JP
Nouv Rev Fr Hematol (1978); 1989; 31(3):193-202. PubMed ID: 2575737
[TBL] [Abstract][Full Text] [Related]
33. Molecular genetics of hemophilia A.
Gitschier J
Schweiz Med Wochenschr; 1989 Sep; 119(39):1329-31. PubMed ID: 2508218
[TBL] [Abstract][Full Text] [Related]
34. Usefulness of determination of factor VIII intron 7 polymorphism by a non-radioactive technique for carrier detection of hemophilia A.
Sacchi E; Stefanile C; Tagliavacca L; Mannucci PM; Bianchi Bonomi A
Thromb Haemost; 1992 Nov; 68(5):622-3. PubMed ID: 1455412
[No Abstract] [Full Text] [Related]
35. [Detection of hemophilia A gene carriers in a Brazilian population].
Arruda VR; Annichino-Bizzacchi JM; Costa FF
Rev Assoc Med Bras (1992); 1993; 39(3):126-30. PubMed ID: 7904214
[TBL] [Abstract][Full Text] [Related]
36. Genetic counseling of hemophilia carriers.
Ljung R; Tedgård U
Semin Thromb Hemost; 2003 Feb; 29(1):31-6. PubMed ID: 12640562
[TBL] [Abstract][Full Text] [Related]
37. [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]
38. 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]
39. 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]
40. 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]
[Previous] [Next] [New Search]
