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American Journal of Medical Genetics|August 9, 1996
Tissue-specific methylation differences and cognitive function in fragile X premutation femalesD J Allingham-Hawkins, C A Brown, R Babul, et al.American Journal of Human Genetics|August 1, 1992
Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosomeJ T Clarke, P J Wilson, C P Morris, et al.Journal of Medical Microbiology|October 13, 2006
Detection of enteroaggregative Escherichia coli in faecal samples from patients in the community with diarrhoeaClaire Jenkins, Mathias Tembo, Henrik Chart, et al.British Medical Bulletin|July 1, 1989
Myogenic regulation of dystrophin gene expressionH J Klamut, E E Zubrzycka-Gaarn, D E Bulman, et al.Cytogenetic and Genome Research|April 1, 2006
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.Inorganic Chemistry|October 15, 2024
Innovative N-Acridine Thiosemicarbazones and Their Zn(II) Complexes Transmetallate with Cu(II): Redox Activity and Suppression of Detrimental Oxy-Myoglobin OxidationBusra Kaya, Henry Smith, Yanbing Chen, et al.Neurogenetics|June 5, 2013
Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.Gene|November 14, 1998
Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin geneJ C McNaughton, D J Cockburn, G Hughes, et al.American Journal of Human Genetics|June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.Neurogenetics|March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.Pageof 12