175 related articles for article (PubMed ID: 1356752)
21. Carrier detection and gene analysis of Duchenne muscular dystrophy.
Pearson PL; van Ommen GJ; Bakker E
Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():353-8. PubMed ID: 2884063
[No Abstract] [Full Text] [Related]
22. Molecular probe protocol for determining carrier status in Duchenne and Becker muscular dystrophies.
Prior TW; Friedman KJ; Highsmith WE; Perry TR; Silverman LM
Clin Chem; 1990 Mar; 36(3):441-5. PubMed ID: 1968788
[TBL] [Abstract][Full Text] [Related]
23. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
Darras BT; Koenig M; Kunkel LM; Francke U
Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
[TBL] [Abstract][Full Text] [Related]
24. DNA probes for carrier identification in Duchenne muscular dystrophy.
Worton RG
Clin Chem; 1989 Apr; 35(4):519-20. PubMed ID: 2564816
[No Abstract] [Full Text] [Related]
25. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
Hejtmancik JF; Harris SG; Tsao CC; Ward PA; Caskey CT
Neurology; 1986 Dec; 36(12):1553-62. PubMed ID: 2878392
[TBL] [Abstract][Full Text] [Related]
26. The value of deletion analysis for carrier detection in Duchenne muscular dystrophy (DMD).
Bejjani B; Finn P; Milunsky A; Amos J
Clin Genet; 1991 Apr; 39(4):245-52. PubMed ID: 2070545
[TBL] [Abstract][Full Text] [Related]
27. Prenatal testing for Duchenne and Becker muscular dystrophy.
Cole CG; Walker A; Coyne A; Johnson L; Hart KA; Hodgson S; Sheridan R; Bobrow M
Lancet; 1988 Feb; 1(8580):262-6. PubMed ID: 2893082
[TBL] [Abstract][Full Text] [Related]
28. Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
Thompson MW; Ray PN; Belfall B; Duff C; Logan C; Oss I; Worton RG
J Med Genet; 1986 Dec; 23(6):548-55. PubMed ID: 2879926
[TBL] [Abstract][Full Text] [Related]
29. Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.
Speer A; Spiegler AW; Hanke R; Grade K; Giertler U; Schieck J; Forrest S; Davies KE; Neumann R; Bollmann R
J Med Genet; 1989 Jan; 26(1):1-5. PubMed ID: 2918522
[TBL] [Abstract][Full Text] [Related]
30. Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy.
Roberts RG; Cole CG; Hart KA; Bobrow M; Bentley DR
Nucleic Acids Res; 1989 Jan; 17(2):811. PubMed ID: 2563578
[No Abstract] [Full Text] [Related]
31. Antenatal diagnosis.
Old JM; Ludlam CA
Baillieres Clin Haematol; 1991 Apr; 4(2):391-428. PubMed ID: 1680511
[No Abstract] [Full Text] [Related]
32. Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy.
Speer MC; Pericak-Vance MA; Yamaoka LH; Koh J; Hung WY; Gaskell PC; Vance JM; Bartlett RJ; Roses AD
Prenat Diagn; 1988 Jul; 8(6):427-37. PubMed ID: 3211845
[TBL] [Abstract][Full Text] [Related]
33. Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studies.
Prior TW; Blasco PA; Dove JL; Leshner RT; Gruemer HD
Clin Chem; 1989 Apr; 35(4):679-83. PubMed ID: 2564818
[TBL] [Abstract][Full Text] [Related]
34. Evaluation of DNA-based diagnosis for haemophilia A.
Wadelius C; Blombäck M; Goonewardena P; Anvret M; Lindstedt M; Gustavson KH; Pettersson U
Scand J Clin Lab Invest; 1991 Nov; 51(7):625-33. PubMed ID: 1810022
[TBL] [Abstract][Full Text] [Related]
35. [Hemophilia and Duchenne de Boulogne myopathy. Genetics].
Battin J; Serville F
Rev Prat; 1994 Sep; 44(14):1955-60. PubMed ID: 7939289
[No Abstract] [Full Text] [Related]
36. Somatic mosaicism at the Duchenne locus.
Lebo RV; Olney RK; Golbus MS
Am J Med Genet; 1990 Oct; 37(2):187-90. PubMed ID: 1978985
[TBL] [Abstract][Full Text] [Related]
37. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.
Bakker E; Hofker MH; Goor N; Mandel JL; Wrogemann K; Davies KE; Kunkel LM; Willard HF; Fenton WA; Sandkuyl L
Lancet; 1985 Mar; 1(8430):655-8. PubMed ID: 2858615
[TBL] [Abstract][Full Text] [Related]
38. [Molecular biology in diagnosis and detection of deletion in Duchenne muscular dystrophy].
Graninger W; Wintersberger W; Meron G; Smolen J; Toifl K; Vormittag W
Wien Klin Wochenschr; 1991; 103(7):207-9. PubMed ID: 2063586
[TBL] [Abstract][Full Text] [Related]
39. X-chromosome-specific probe DX13 for carrier detection and first trimester prenatal diagnosis in haemophilia A.
Tønnesen T; Søndergaard F; Mikkelsen M; Davies KE; Old J; Winter RM; Hauge M
Lancet; 1984 Dec; 2(8414):1269-70. PubMed ID: 6150293
[No Abstract] [Full Text] [Related]
40. Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy.
Yau SC; Roberts RG; Bobrow M; Mathew CG
Lancet; 1993 Jan; 341(8840):273-5. PubMed ID: 8093919
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]