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American Journal of Medical Genetics|February 1, 1988
Marfan syndrome: exclusion of genetic linkage to three major collagen genesC A Francomano, E A Streeten, D A Meyers, et al.American Journal of Human Genetics|September 1, 1987
Mortality in achondroplasiaJ T Hecht, C A Francomano, W A Horton, et al.Genomics|June 1, 1990
Use of denaturing gradient gel electrophoresis for detection of mutation and prospective diagnosis in late onset ornithine transcarbamylase deficiencyJ E Finkelstein, C A Francomano, S W Brusilow, et al.American Journal of Medical Genetics|July 16, 1999
Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasiaM Deere, T Sanford, C A Francomano, et al.Molecular and Cellular Biology|May 1, 1989
Differential expression in male and female mouse liver of very similar mRNAs specified by two group 1 major urinary protein genesI McIntosh, J O BishopFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1992
Cystic fibrosis transmembrane conductance regulator and the etiology and pathogenesis of cystic fibrosisI McIntosh, G R CuttingHuman Molecular Genetics|May 23, 1998
Identification of a mutation in liver glycogen phosphorylase in glycogen storage disease type VIS Chang, M J Rosenberg, H Morton, et al.Clinical Genetics|October 31, 2001
Living with Marfan syndrome I. Perceptions of the conditionK F Peters, F Kong, R Horne, et al.American Journal of Medical Genetics|March 14, 2002
Comprehensive resource: Skeletal gene databaseL Jia, N C Ho, S S Park, et al.Clinical Genetics|October 31, 2001
Living with Marfan syndrome II. Medication adherence and physical activity modificationK F Peters, R Horne, F Kong, et al.Pageof 17