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Human Molecular Genetics|September 4, 2003
Williams-Beuren syndrome: a challenge for genotype-phenotype correlationsM TassabehjiAgeing Research Reviews|July 3, 2004
Iron and ageing: an introduction to iron regulatory mechanismsCathy W Levenson, Nadine M TassabehjiPCR Methods and Applications|February 1, 1992
A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiencyS Collier, M Tassabehji, T StrachanJournal of Dental Education|February 15, 2024
Pre-doctoral dental students' knowledge, training, perceptions, and attitudes regarding obesity and treatments: A survey studyTamara Biary, Mathew Finkelman, Nadine M TassabehjiNature Genetics|November 1, 1994
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) geneM Tassabehji, V E Newton, A P ReadNature Genetics|March 1, 1993
A de novo pathological point mutation at the 21-hydroxylase locus: implications for gene conversion in the human genomeS Collier, M Tassabehji, P Sinnott, et al.Experimental Biology and Medicine (Maywood, N.J.)|October 26, 2005
Copper alters the conformation and transcriptional activity of the tumor suppressor protein p53 in human Hep G2 cellsNadine M Tassabehji, Jacob W VanLandingham, Cathy W LevensonCompendium of Continuing Education in Dentistry (Jamesburg, N.J. : 1995)|September 14, 2024
The Role of Proper Nutrition for Patients Undergoing Periodontal Surgery: A Scoping ReviewNadine M Tassabehji, Yu-Fang Lao, Irina F DraganPhysiology & Behavior|July 29, 2008
Zinc deficiency induces depression-like symptoms in adult ratsNadine M Tassabehji, Rikki S Corniola, Almamoun Alshingiti, et al.European Journal of Human Genetics : EJHG|May 30, 2003
Mutations in PAX1 may be associated with Klippel-Feil syndromeJ M McGaughran, A Oates, D Donnai, et al.Pageof 4