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Developmental Medicine and Child Neurology|August 1, 1994
Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxiaS Bundey, C Hardy, S Vickers, et al.Nucleic Acids Research|January 25, 1992
The human insulin gene linked polymorphic region exhibits an altered DNA structureM C Hammond-Kosack, B Dobrinski, R Lurz, et al.American Journal of Human Genetics|June 7, 2000
Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27P Ianakiev, M W Kilpatrick, I Toudjarska, et al.Lancet (London, England)|March 7, 1992
Location of gene for Gorlin syndromeP A Farndon, R G Del Mastro, D G Evans, et al.The Journal of Biological Chemistry|August 25, 1986
Unusual DNA structures in the adenovirus genomeM W Kilpatrick, A Torri, D S Kang, et al.The British Journal of Ophthalmology|March 1, 1993
X linked exudative vitreoretinopathy: clinical features and genetic linkage analysisP Fullwood, J Jones, S Bundey, et al.Nucleic Acids Research|October 25, 1982
The nucleotide sequence of the 5S rRNA from Spiroplasma species BC3 and Mycoplasma mycoides sp. capri PG3R T Walker, E T Chelton, M W Kilpatrick, et al.Ocular Immunology and Inflammation|July 26, 2012
The detection of herpesviral DNA in aqueous fluid samples from patients with Fuchs' heterochromic cyclitisS M Mitchell, L Phylactou, J D Fox, et al.Journal of Medical Genetics|March 1, 1995
A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndromeT Webb, D Clarke, C A Hardy, et al.Gene Therapy|October 21, 2003
Enhanced intracellular availability and survival of hammerhead ribozymes increases target ablation in a cellular model of osteogenesis imperfectaY Smicun, M W Kilpatrick, J Florer, et al.Pageof 5