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Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.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.Archives of Oral Biology|February 13, 2002
A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfectaS R Greene, Z A Yuan, J T Wright, et al.British Journal of Cancer|April 1, 1990
Fatty acid control of growth of human cervical and endometrial cancer cellsR P Gleeson, M Ayub, J T Wright, et al.Journal of Dental Research|March 27, 2007
Transgenic mice that express normal and mutated amelogeninsC W Gibson, Z A Yuan, Y Li, et al.Controlled Clinical Trials|August 1, 1996
Design and baseline characteristics of participants in the African American Study of Kidney Disease and Hypertension (AASK) Pilot StudyJ T Wright, J W Kusek, R D Toto, 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.International Journal of Technology Assessment in Health Care|January 1, 1992
The Cleveland Veterans Affairs Medical Center firm systemC S Landefeld, G E Rosenthal, J Aucott, et al.Journal of Dental Research|January 1, 2010
The amelogenin C-terminus is required for enamel developmentM K Pugach, Y Li, C Suggs, et al.Pageof 25