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5. [DNA diagnosis of Duchenne muscular dystrophy]. Matsumoto T No To Shinkei; 1991 May; 43(5):421-8. PubMed ID: 1680358 [No Abstract] [Full Text] [Related]
6. Genetic counseling of isolated carriers of Duchenne muscular dystrophy. Hoffman EP; Pegoraro E; Scacheri P; Burns RG; Taber JW; Weiss L; Spiro A; Blattner P Am J Med Genet; 1996 Jun; 63(4):573-80. PubMed ID: 8826437 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Analysis of deletion mutations of the dystrophin gene by the multiplex polymerase chain reaction method in the diagnosis of Duchenne muscular dystrophy]. Baranov Vs; Gorbunova VN; Malysheva OV; Krasil'nikov VV Mol Gen Mikrobiol Virusol; 1991 Sep; (9):13-5. PubMed ID: 1745268 [TBL] [Abstract][Full Text] [Related]
9. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients. Shomrat R; Gluck E; Legum C; Shiloh Y Am J Med Genet; 1994 Feb; 49(4):369-73. PubMed ID: 8160727 [TBL] [Abstract][Full Text] [Related]
10. [Lessons of dystrophin]. Desnuelle C Presse Med; 1994 May; 23(19):896-900. PubMed ID: 7937619 [TBL] [Abstract][Full Text] [Related]
11. [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]
12. [Deletions within the gene of dystrophin in Duchenne and Becker muscular dystrophy]. Zimowski JG; Bisko M; Fidziańska E; Hausmanowa-Petrusewicz I; Badurska B; Borkowska J; Lusakowska A; Fidziańska A; Jezuita J; Zaremba J Neurol Neurochir Pol; 1993; 27(4):469-78. PubMed ID: 8247234 [TBL] [Abstract][Full Text] [Related]
14. Experience and strategy for the molecular testing of Duchenne muscular dystrophy. Prior TW; Bridgeman SJ J Mol Diagn; 2005 Aug; 7(3):317-26. PubMed ID: 16049303 [TBL] [Abstract][Full Text] [Related]
15. Dystrophin analysis in the diagnosis of muscular dystrophy. Norman AM; Hughes HE; Gardner-Medwin D; Nicholson LV Arch Dis Child; 1989 Oct; 64(10):1501-3. PubMed ID: 2684033 [TBL] [Abstract][Full Text] [Related]
16. Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy. Shomrat R; Driks N; Legum C; Shiloh Y Am J Med Genet; 1992 Feb; 42(3):281-7. PubMed ID: 1536162 [TBL] [Abstract][Full Text] [Related]
18. Dystrophin-associated proteins and the muscular dystrophies. Brown RH Annu Rev Med; 1997; 48():457-66. PubMed ID: 9046976 [TBL] [Abstract][Full Text] [Related]
19. Failure of early diagnosis in symptomatic Duchenne muscular dystrophy. Bushby KM; Hill A; Steele JG Lancet; 1999 Feb; 353(9152):557-8. PubMed ID: 10028989 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]