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Human Molecular Genetics|March 21, 1998
Genetic linkage of the tricho-dento-osseous syndrome to chromosome 17q21T C Hart, D W Bowden, J Bolyard, et al.American Journal of Human Genetics|March 21, 2000
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27V Shashi, M N Berry, S Shoaf, et al.Journal of Dental Research|October 26, 2005
Phenotype of ENAM mutations is dosage-dependentD Ozdemir, P S Hart, E Firatli, et al.Human Molecular Genetics|April 18, 1998
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndromeJ A Price, D W Bowden, J T Wright, et al.Journal of Dental Research|November 26, 2008
Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfectaD A McKnight, J P Simmer, P S Hart, et al.Journal of the California Dental Association|October 29, 1998
Reducing the burden of oral and pharyngeal cancersD M Winn, A L Sandberg, A M Horowitz, et al.Human Genetics|December 1, 1992
Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell lineJ E Reynolds, J A Fletcher, C H Lytle, et al.Journal of the American Dental Association (1939)|June 19, 1998
Scientific progress in understanding oral and pharyngeal cancersD M Winn, S R Diehl, A M Horowitz, et al.Calcified Tissue International|January 11, 2003
Aquaporin expression in developing human teeth and selected orofacial tissuesW Wang, P S Hart, N P Piesco, et al.Molecular Genetics and Metabolism|June 27, 2002
Identification of a novel cathepsin C mutation (p.W185X) in a Brazilian kindred with Papillon-Lefèvre syndromeP S Hart, D Pallos, Y Zhang, et al.Pageof 11