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The Journal of Clinical Investigation|October 1, 1989
Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotypeB J Starman, D Eyre, H Charbonneau, et al.Nature Genetics|March 18, 1999
Heterozygous mutations in the gene encoding noggin affect human joint morphogenesisY Gong, D Krakow, J Marcelino, et al.American Journal of Human Genetics|April 16, 1998
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrumM D Briggs, G R Mortier, W G Cole, et al.American Journal of Medical Genetics|December 25, 1991
Radiological findings in Hallermann-Streiff syndrome: report of five cases and a review of the literatureC L Christian, R S Lachman, A S Aylsworth, et al.Behavioural Brain Research|January 1, 1982
Analysis of facial displays and verbal report to assess subjective state in the non-invasive detection of limbic system activation by procaine hydrochlorideC Stark-Adamec, R E Adamec, J M Graham, et al.American Journal of Medical Genetics|January 1, 1991
Congenital gastric teratoma in Wiedemann-Beckwith syndromeT C Falik-Borenstein, J R Korenberg, I Davos, et al.American Journal of Medical Genetics|November 15, 1993
Congenital diaphragmatic hernia in the Brachmann-de Lange syndromeC Cunniff, C J Curry, J C Carey, et al.Pharmacogenetics|March 30, 2000
Association study of dopamine receptor gene polymorphisms with drug-induced hallucinations in patients with idiopathic Parkinson's diseaseA J Makoff, J M Graham, M J Arranz, et al.Journal of Medical Genetics|September 13, 2005
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 geneK P Hoornaert, C Dewinter, I Vereecke, et al.Microbial Ecology|February 8, 2005
Annual patterns in bacterioplankton community variability in a humic lakeA D Kent, S E Jones, A C Yannarell, et al.Pageof 42