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Journal of Dental Research|July 15, 1998
HLA-DR alleles are associated with IDDM, but not with impaired neutrophil chemotaxis in IDDMC J Gustke, S H Stein, T C Hart, et al.American Journal of Human Genetics|May 11, 1992
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortiumL A Farrer, K M Grundfast, J Amos, et al.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.Journal of Medical Genetics|September 1, 1987
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8S R Diehl, M Boehnke, F S Collins, et al.American Journal of Medical Genetics|July 17, 1995
Analysis of variability of clinical manifestations in Waardenburg syndromeJ E Reynolds, J M Meyer, B Landa, et al.Human Molecular Genetics|April 1, 1996
Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?A Pandya, X J Xia, B L Landa, et al.Journal of Periodontology|December 29, 2000
Evidence of a substantial genetic basis for risk of adult periodontitisB S Michalowicz, S R Diehl, J C Gunsolley, et al.Oral Diseases|October 22, 2008
Oral and dental phenotype of dyskeratosis congenitaJ C Atkinson, K E Harvey, D L Domingo, 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 Medical Genetics|December 20, 2003
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defectsT C Hart, P S Hart, M C Gorry, et al.Pageof 11