172 related articles for article (PubMed ID: 2893082)
1. 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]
2. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
Lindlöf M; Kääriäinen H; Davies KE; de la Chapelle A
J Med Genet; 1986 Dec; 23(6):560-72. PubMed ID: 2879928
[TBL] [Abstract][Full Text] [Related]
3. The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratory.
Laing NG; Mears ME; Chandler DC; Layton MG; Thomas HE; Johnsen RD; Goldblatt J; Kakulas BA
Med J Aust; 1991 Jan; 154(1):14-8. PubMed ID: 1670611
[TBL] [Abstract][Full Text] [Related]
4. The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.
Hodgson S; Walker A; Cole C; Hart K; Johnson L; Heckmatt J; Dubowitz V; Bobrow M
J Med Genet; 1987 Mar; 24(3):152-9. PubMed ID: 3572997
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 deoxyribonucleic acid probes.
Katayama S; Montano M; Slotnick RN; Lebo RV; Golbus MS
Am J Obstet Gynecol; 1988 Mar; 158(3 Pt 1):548-55. PubMed ID: 2894769
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving field.
Bakker E; Bonten EJ; Veenema H; den Dunnen JT; Grootscholten PM; van Ommen GJ; Pearson PL
J Inherit Metab Dis; 1989; 12 Suppl 1():174-90. PubMed ID: 2509804
[TBL] [Abstract][Full Text] [Related]
8. Linkage studies in Duchenne and Becker muscular dystrophies.
Walker A; Hart K; Cole C; Hodgson S; Johnson L; Dubowitz V; Bobrow M
J Med Genet; 1986 Dec; 23(6):538-47. PubMed ID: 2879925
[TBL] [Abstract][Full Text] [Related]
9. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
Bakker E; Bonten EJ; De Lange LF; Veenema H; Majoor-Krakauer D; Hofker MH; Van Ommen GJ; Pearson PL
J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of Duchenne muscular dystrophy by polymerase chain reaction analysis.
Katayama S; Takeshita N; Yano T; Katagiri Y; Shirosita Y; Kubo H; Hirakawa S; Ubagai T
Fetal Diagn Ther; 1994; 9(6):379-84. PubMed ID: 7880434
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis in Becker muscular dystrophy.
Wood S; Shukin RJ; Yong SL; Wilson D; Kalousek D; Chudley A
Clin Genet; 1987 Jan; 31(1):45-7. PubMed ID: 2882880
[TBL] [Abstract][Full Text] [Related]
12. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
Tuffery S; Moine P; Sarda P; Lefort G; Boulot P; Demaille J; Claustres M
Genet Couns; 1994; 5(2):183-5. PubMed ID: 7917130
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.
Old JM; Davies KE
J Med Genet; 1986 Dec; 23(6):556-9. PubMed ID: 2879927
[TBL] [Abstract][Full Text] [Related]
14. [Prenatal diagnosis of Duchenne muscular dystrophy using DNA RFLP analysis].
Zeng YT
Zhonghua Yi Xue Za Zhi; 1988 Oct; 68(10):565-7, 38. PubMed ID: 2907413
[No Abstract] [Full Text] [Related]
15. Molecular biological approaches to genetic disorders in prenatal diagnosis.
Katayama S
Early Hum Dev; 1992; 29(1-3):149-53. PubMed ID: 1356752
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected male.
Chen JD; Denton MJ; Serravalle S; Morgan G
Aust Paediatr J; 1988 Dec; 24(6):351-3. PubMed ID: 2907402
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of Duchenne and Becker muscular dystrophy.
Abbs S
Prenat Diagn; 1996 Dec; 16(13):1187-98. PubMed ID: 9061750
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy by PCR methods].
Tsukamoto H; Inui K; Okada S
Nihon Rinsho; 1993 Sep; 51(9):2428-34. PubMed ID: 8105117
[TBL] [Abstract][Full Text] [Related]
20. [Prenatal DNA-diagnosis of Duchenne muscular dystrophy].
Evgrafov OV; Poliakov AV; Zaĭtseva SP; Vinogradov SV; Bakharev VA; Mil'man FA; Lisova LP; Zaretskaia NV; Malygina NA; Badalian LO
Mol Gen Mikrobiol Virusol; 1991 Feb; (2):15-6. PubMed ID: 1674355
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
