140 related articles for article (PubMed ID: 8400866)
1. Report on the 16th ENMC workshop--carrier diagnosis of Duchenne and Becker muscular dystrophy.
Abbs S; Bobrow M
Neuromuscul Disord; 1993 May; 3(3):241-2. PubMed ID: 8400866
[No Abstract] [Full Text] [Related]
2. A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales.
Norman A; Harper P
Clin Genet; 1989 Jul; 36(1):31-7. PubMed ID: 2766561
[TBL] [Abstract][Full Text] [Related]
3. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
Spiegler AW; Huppert P; Werner W; Metzke H; Strobel U; Köhler K; Gerhardt R; Kaufmann J; Herrmann FH
Z Arztl Fortbild (Jena); 1988; 82(22):1139-42. PubMed ID: 3247797
[No Abstract] [Full Text] [Related]
4. Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis.
Bakker E; Bonten EJ; den Dunnen JT; Veenema H; Grootscholten PM; van Ommen GJ; Pearson PL
Prog Clin Biol Res; 1989; 306():51-67. PubMed ID: 2662213
[No Abstract] [Full Text] [Related]
5. Genetic analysis of the Duchenne muscular dystrophy gene.
Prior TW
Arch Pathol Lab Med; 1991 Oct; 115(10):984-90. PubMed ID: 1898245
[TBL] [Abstract][Full Text] [Related]
6. Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican families.
Arenas D; Coral R; Cisneros B; Peñaloza L; Salamanca F; Kofman S; Mercado R; Méndez J; Martínez C; Montañez C
Arch Med Res; 1996; 27(2):151-6. PubMed ID: 8696057
[TBL] [Abstract][Full Text] [Related]
7. The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.
van Essen AJ; Kneppers AL; van der Hout AH; Scheffer H; Ginjaar IB; ten Kate LP; van Ommen GJ; Buys CH; Bakker E
J Med Genet; 1997 Oct; 34(10):805-12. PubMed ID: 9350811
[TBL] [Abstract][Full Text] [Related]
8. Editorial: Carrier detection in Duchenne type muscular dystrophy.
Morgan G
Aust N Z J Med; 1974 Apr; 4(2):196-7. PubMed ID: 4528526
[No Abstract] [Full Text] [Related]
9. [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]
10. Perspectives and molecular diagnosis of Duchenne and Becker muscular dystrophies.
Prior TW
Clin Lab Med; 1995 Dec; 15(4):927-41. PubMed ID: 8838231
[TBL] [Abstract][Full Text] [Related]
11. Potential pitfalls in using DNA probes to counsel Duchenne and Becker muscular dystrophy families.
Shi YJ; Fischbeck KH; Ritter A
Chin Med J (Engl); 1992 Jun; 105(6):469-75. PubMed ID: 1451547
[TBL] [Abstract][Full Text] [Related]
12. Systemic membrane defect in the proximal muscular dystrophies.
Pickard NA; Gruemer HD; Verrill HL; Isaacs ER; Robinow M; Nance WE; Myers EC; Goldsmith B
N Engl J Med; 1978 Oct; 299(16):841-6. PubMed ID: 308614
[TBL] [Abstract][Full Text] [Related]
13. Distinction between Duchenne and other muscular dystrophies by ribosomal protein synthesis.
Ionasescu V
J Med Genet; 1975 Mar; 12(1):49-54. PubMed ID: 164552
[TBL] [Abstract][Full Text] [Related]
14. Deletion analysis for Duchenne (and Becker) muscular dystrophy.
Kimber RD; Hyland VJ; Haan EA; Mulley JC
Aust Paediatr J; 1989 Oct; 25(5):292-5. PubMed ID: 2590130
[TBL] [Abstract][Full Text] [Related]
15. [A two-year-old clinically manifesting carrier of Duchenne muscular dystrophy].
Yamamoto T; Kawahara H; Inagaki M; Ohta S
No To Hattatsu; 1991 Jul; 23(4):384-8. PubMed ID: 1873056
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. High frequency of new mutations in North Indian Duchenne/Becker muscular dystrophy patients.
Sinha S; Mishra S; Singh V; Mittal RD; Mittal B
Clin Genet; 1996 Nov; 50(5):327-31. PubMed ID: 9007319
[TBL] [Abstract][Full Text] [Related]
18. Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families.
Bachrati CZ; Somodi Z; Endreffy E; Kalmár T; Raskó I
Ann Hum Genet; 1998 Nov; 62(Pt 6):511-20. PubMed ID: 10363129
[TBL] [Abstract][Full Text] [Related]
19. Muscular dystrophies and other genetic myopathies.
Shieh PB
Neurol Clin; 2013 Nov; 31(4):1009-29. PubMed ID: 24176421
[TBL] [Abstract][Full Text] [Related]
20. Dystrophin immunohistochemistry in a symptomatic carrier of Becker muscular dystrophy.
Haginoya K; Yamamoto K; Iinuma K; Yanagisawa T; Ichinohasama Y; Shimmoto M; Suzuki Y; Tada K
J Neurol; 1991 Oct; 238(7):375-8. PubMed ID: 1683669
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
