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279 related items for PubMed ID: 8411068
21. The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities. Bushby KM, Gardner-Medwin D, Nicholson LV, Johnson MA, Haggerty ID, Cleghorn NJ, Harris JB, Bhattacharya SS. J Neurol; 1993 Feb; 240(2):105-12. PubMed ID: 8437017 [Abstract] [Full Text] [Related]
22. Very mild muscular dystrophy associated with the deletion of 46% of dystrophin. England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE. Nature; 1990 Jan 11; 343(6254):180-2. PubMed ID: 2404210 [Abstract] [Full Text] [Related]
23. Detection of DMD gene deletions in Thai children patients. Kamolsilp M, Paditaporn R, Noonai A, Wasant P. Southeast Asian J Trop Med Public Health; 1995 Jan 11; 26 Suppl 1():172-4. PubMed ID: 8629100 [Abstract] [Full Text] [Related]
31. Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients. Hassan MJ, Mahmood S, Ali G, Bibi N, Waheed I, Rafiq MA, Ansar M, Ahmad W. Pediatr Int; 2008 Apr 11; 50(2):162-6. PubMed ID: 18353051 [Abstract] [Full Text] [Related]
35. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy. Zimowski JG, Massalska D, Holding M, Jadczak S, Fidziańska E, Lusakowska A, Kostera-Pruszczyk A, Kamińska A, Zaremba J. Neurol Neurochir Pol; 2014 Jul 11; 48(6):416-22. PubMed ID: 25482253 [Abstract] [Full Text] [Related]