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Experimental & Molecular Medicine|January 25, 2002
Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patientsL S Chaturvedi, M Mukherjee, S Srivastava, et al.Experimental & Molecular Medicine|May 20, 2003
De novo mutations in sporadic deletional Duchenne muscular dystrophy (DMD) casesMonisha Mukherjee, L S Chaturvedi, Sandhya Srivastava, et al.Human Genetics|February 1, 1997
Proportion and pattern of dystrophin gene deletions in north Indian Duchenne and Becker muscular dystrophy patientsV Singh, S Sinha, S Mishra, et al.The Indian Journal of Medical Research|March 31, 2001
Carrier detection in non-deletional Duchenne/Becker muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin geneL S Chaturvedi, S Srivastava, M Mukherjee, et al.The Indian Journal of Medical Research|January 1, 1997
Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at LucknowB Mittal, V Singh, S Mishra, et al.Pageof 1