242 related articles for article (PubMed ID: 3127923)
1. Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A.
Sampietro M; Camerino G; Romano M; Cappellini MD; Fiorelli G; Brambati B; Guerneri S; Ferrari M; Travi M; Krachmalnicoff A
Thromb Haemost; 1987 Dec; 58(4):988-92. PubMed ID: 3127923
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Prenatal diagnosis of classic hemophilia.
Firshein SI; Hoyer LW; Lazarchick J; Forget BG; Hobbins JC; Clyne LP; Pitlick FA; Muir WA; Merkatz IR; Mahoney MJ
N Engl J Med; 1979 Apr; 300(17):937-41. PubMed ID: 431560
[TBL] [Abstract][Full Text] [Related]
5. First-trimester prenatal diagnosis in haemophilia A and B families--10 years experience from a centre in India.
Shetty S; Ghosh K; Jijina F
Prenat Diagn; 2006 Nov; 26(11):1015-7. PubMed ID: 16941728
[TBL] [Abstract][Full Text] [Related]
6. Hemophilia A carrier detection by restriction fragment length polymorphism analysis and discriminant analysis based on ELISA of factor VIII and vWf.
Poon MC; Hoar DI; Low S; Pon JK; Anand S; Sinclair GD
J Lab Clin Med; 1992 Jun; 119(6):751-62. PubMed ID: 1350611
[TBL] [Abstract][Full Text] [Related]
7. 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]
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. Carrier detection and prenatal diagnosis in haemophilia A and B.
Chistolini A; Papacchini M; Mazzucconi MG; La Verde G; Arcieri R; Ferrari A; Paesano R; Pachi A; Mariani G
Haematologica; 1990; 75(5):424-8. PubMed ID: 1982946
[TBL] [Abstract][Full Text] [Related]
10. [Possibilities of prenatal diagnosis in hemophilia A based on DNA analysis].
Németi M; Bolodár A; Török O; Papp Z
Orv Hetil; 1990 Jul; 131(30):1635-8. PubMed ID: 2119490
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. [Prenatal diagnosis of hemophilia A by DNA analysis].
Wu G
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Dec; 13(6):428-34. PubMed ID: 1686577
[TBL] [Abstract][Full Text] [Related]
13. Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphisms.
Bröcker-Vriends AH; Briët E; Quadt R; Dreesen JC; Bakker E; Claassen-Tegelaar R; Kanhai HH; van de Kamp JJ; Pearson PL
Thromb Haemost; 1987 Apr; 57(2):131-6. PubMed ID: 2885943
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis in a haemophilia A family by both factor VIII activity and antigen measurements.
Shetty S; Ghosh K; Mohanty D
J Assoc Physicians India; 2003 Sep; 51():916-8. PubMed ID: 14710984
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDR.
Herrmann FH; Kruse T; Wehnert M; Vogel G; Wulff K
Folia Haematol Int Mag Klin Morphol Blutforsch; 1988; 115(4):489-93. PubMed ID: 2465959
[TBL] [Abstract][Full Text] [Related]
18. Haemophilia management: the application of DNA analysis for prenatal diagnosis.
Van de Water NS; Ockelford PA; Berry EW; Browett PJ
N Z Med J; 1991 Oct; 104(922):443-6. PubMed ID: 1681487
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. [Gene diagnosis of hemophilia A by PCR].
Feng J
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Oct; 13(5):384-8. PubMed ID: 1839260
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]