224 related articles for article (PubMed ID: 7902217)
21. 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]
22. DNA-based prenatal diagnosis of heritable skin diseases.
Christiano AM; Uitto J
Arch Dermatol; 1993 Nov; 129(11):1455-9. PubMed ID: 7902070
[TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction (PCR). Comparison of conventional RFLP methods with PCR used in combination with allele specific oligonucleotides or RFLP analysis.
Schwartz M; Petersen KB; Gregersen N; Hinkel K; Newton CR
Clin Genet; 1989 Dec; 36(6):419-26. PubMed ID: 2574085
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center.
Sacchi E; Randi AM; Tagliavacca L; Sampietro M; Primignani P; Mannucci PM
Int J Clin Lab Res; 1992; 21(4):310-3. PubMed ID: 1350470
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. [Prenatal diagnosis of hemophilia A in the 2d trimester and its problems].
Sedlácek Z; Macek M; Chudoba D; Hájek Z; Sedinová M
Cas Lek Cesk; 1988 Jan; 127(4):113-6. PubMed ID: 2894896
[No Abstract] [Full Text] [Related]
28. [Gene mutation and gene diagnosis of hemophilia].
Kojima T
Nihon Seirigaku Zasshi; 1998; 60(1):31-42. PubMed ID: 9614303
[No Abstract] [Full Text] [Related]
29. Prenatal exclusion testing for Huntington disease using the polymerase chain reaction.
McIntosh I; Curtis A; Millan FA; Brock DJ
Am J Med Genet; 1989 Feb; 32(2):274-6. PubMed ID: 2564738
[TBL] [Abstract][Full Text] [Related]
30. [Initial experience with the diagnosis of hemophilia A using molecular genetics].
Sedlácek Z; Macek M; Malcolm S; Fisher J; Chudoba D; Hirsch I; Goetz P
Cas Lek Cesk; 1987 May; 126(22):682-6. PubMed ID: 2885094
[No Abstract] [Full Text] [Related]
31. Prenatal diagnosis of hemophilia involving grandpaternal mosaicism.
Lebo RV; Koerper MA; Kim JH; Chueh J; Golbus MS
Am J Med Genet; 1993 Sep; 47(3):401-4. PubMed ID: 7907841
[TBL] [Abstract][Full Text] [Related]
32. Carrier detection and prenatal diagnosis in 98 families of haemophilia A by linkage analysis and direct detection of mutations.
Lavergne JM; Laurian Y; Dudilleux A; Larrieu MJ; Bahnak BR; Meyer D
Blood Coagul Fibrinolysis; 1991 Apr; 2(2):293-301. PubMed ID: 1680009
[TBL] [Abstract][Full Text] [Related]
33. Factor VIII gene mutations and RFLP analysis in hemophilia A.
Krepelová A; Brdicka R; Vorlová Z
Stem Cells; 1993 May; 11 Suppl 1():72-6. PubMed ID: 8100465
[TBL] [Abstract][Full Text] [Related]
34. Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
Gürgey A; Beksaç S; Mesci L; Cakar N; Karakaş U; Kutlar A; Altay C
Turk J Pediatr; 1993; 35(3):159-62. PubMed ID: 7909397
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. Antenatal diagnosis.
Old JM; Ludlam CA
Baillieres Clin Haematol; 1991 Apr; 4(2):391-428. PubMed ID: 1680511
[No Abstract] [Full Text] [Related]
38. Implications of gene sequencing in the direct diagnosis of hemophilia by PCR-RFLP.
Vidal F; Farssac E; Altisent C; Puig L; Gallardo D
Haematologica; 2002 Jan; 87(1):109-10. PubMed ID: 11801473
[No Abstract] [Full Text] [Related]
39. [A case of prenatal diagnosis of beta-thalassemia by polymerase chain reaction].
Kolesnikova TN; Moliaka IuK; Surin VL; Luk'ianenko AV; Asanov AIu; Tagiev AF; Solov'ev GIa
Genetika; 1992 Dec; 28(12):130-4. PubMed ID: 1363470
[TBL] [Abstract][Full Text] [Related]
40. [Clinical molecular-genetics for endocrine and metabolic diseases].
Niikawa N
Rinsho Byori; 1989 Aug; 37(8):847-54. PubMed ID: 2573745
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]