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Journal of Medical Genetics|February 9, 2000
Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin CT C Hart, P S Hart, M D Michalec, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 5, 2008
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic featuresC E Dumitrescu, M H Kelly, A Khosravi, et al.European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|March 11, 2008
Inheritance of occlusal topography: a twin studyC-Y Su, P M Corby, M A Elliot, et al.British Journal of Cancer|November 19, 2011
Correlates of anti-EBV EBNA1 IgA positivity among unaffected relatives from nasopharyngeal carcinoma multiplex familiesC M Chang, K J Yu, W L Hsu, 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|December 10, 1999
Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutationS Beiraghi, A Miller-Chisholm, W J Kimberling, et al.Journal of Clinical Microbiology|November 8, 2005
Microbial risk indicators of early childhood cariesP M Corby, J Lyons-Weiler, W A Bretz, et al.Clinical Nephrology|November 19, 2010
Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisoneA J Bleyer, M Zivná, H Hulková, et al.Journal of Medical Genetics|January 11, 2000
Identification of cathepsin C mutations in ethnically diverse papillon-Lefèvre syndrome patientsP S Hart, Y Zhang, E Firatli, et al.Pageof 11