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Current Opinion in Pediatrics|December 16, 1998
Molecular genetics of long-QT syndromeD Wattanasirichaigoon, A H BeggsTrends in Molecular Medicine|August 23, 2001
Clinical and genetic heterogeneity in nemaline myopathy--a disease of skeletal muscle thin filamentsD Sanoudou, A H BeggsNeuromuscular Disorders : NMD|August 1, 1996
Deficiency of a skeletal muscle isoform of alpha-actinin (alpha-actinin-3) in merosin-positive congenital muscular dystrophyK N North, A H BeggsMolecular and Cellular Biology|June 1, 1989
Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clustersA H Beggs, B R MigeonGene Amplification and Analysis|January 1, 1986
Serum-free selection of onc genesA H Beggs, G A ScangosNeuromuscular Disorders : NMD|January 1, 1992
Early onset autosomal dominant progressive muscular dystrophy presenting in childhood as a Becker phenotype--the importance of dystrophin and molecular genetic analysisG Miller, A H Beggs, J TowfighiJournal of Medical Genetics|January 1, 1994
Exclusion of two candidate loci for autosomal recessive nemaline myopathyE Tahvanainen, A H Beggs, C Wallgren-PetterssonNature|September 1, 1988
Effect of ageing on reactivation of the human X-linked HPRT locusB R Migeon, J Axelman, A H BeggsSomatic Cell and Molecular Genetics|November 1, 1986
Reactivation of X-linked genes in human fibroblasts transformed by origin-defective SV40A H Beggs, J Axelman, B R MigeonThe Journal of General Virology|January 1, 1990
Cell type-specific expression of JC virus T antigen in primary and established cell lines from transgenic miceA H Beggs, J H Miner, G A ScangosPageof 8