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Connective Tissue Research|September 4, 2003
Relationship of phenotype and genotype in X-linked amelogenesis imperfectaJ T Wright, P S Hart, M J Aldred, et al.Developmental Biology|November 11, 2008
In vivo impact of a 4 bp deletion mutation in the DLX3 gene on bone developmentS J Choi, G D Roodman, J Q Feng, et al.Journal of Dental Research|June 1, 2000
Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth developmentC C Hu, T C Hart, B R Dupont, et al.Journal of Craniofacial Genetics and Developmental Biology|March 11, 1998
Dentin dysplasia, type II linkage to chromosome 4qJ A Dean, J K Hartsfield, J T Wright, et al.American Journal of Medical Genetics|October 23, 1997
Analysis of the tricho-dento-osseous syndrome genotype and phenotypeJ T Wright, K Kula, K Hall, et al.Journal of Dental Research|October 26, 2005
Phenotype of ENAM mutations is dosage-dependentD Ozdemir, P S Hart, E Firatli, et al.Journal of Medical Genetics|October 23, 1998
A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina familiesJ A Price, J T Wright, K Kula, et al.Connective Tissue Research|November 4, 2000
Enamel structure and composition in the tricho-dento-osseous syndromeG S Spangler, K I Hall, K Kula, 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.Pageof 36