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Journal of Medical Genetics|February 7, 2001
Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patientsY Zhang, T Lundgren, S Renvert, et al.Oral Oncology|December 20, 2000
Smoking and alcohol in the etiology of oral cancer: gender-specific risk profiles in the south of GreeceA I Zavras, C W Douglass, K Joshipura, et al.American Journal of Human Genetics|October 1, 1994
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypesL A Farrer, K S Arnos, J H Asher, et al.Oral Diseases|February 25, 2009
Hutchinson-Gilford progeria syndrome: oral and craniofacial phenotypesD L Domingo, M I Trujillo, S E Council, et al.Journal of Dental Research|October 26, 2005
Longitudinal analysis of heritability for dental caries traitsW A Bretz, P M Corby, N J Schork, et al.Genomics|December 1, 1987
Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17S R Diehl, M Boehnke, R P Erickson, et al.American Journal of Human Genetics|February 1, 1996
Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndromeJ E Reynolds, M L Marazita, J M Meyer, et al.American Journal of Human Genetics|January 1, 1989
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) geneS R Diehl, M Boehnke, R P Erickson, et al.Genes and Immunity|February 22, 2003
Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patientsY Zhang, R Syed, C Uygar, et al.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.Pageof 11