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T C Hart

Showing results (71-80 of 92) with videos related to

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Journal of Medical Genetics|December 14, 1999
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndromeT C Hart, P S Hart, D W Bowden, et al.
Journal of Medical Genetics|March 4, 2005
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfectaJ-W Kim, J P Simmer, T C Hart, et al.
Clinical Genetics|February 18, 2009
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfectaP S Hart, S Becerik, D Cogulu, et al.
Journal of Medical Genetics|February 9, 2000
Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutationT C Hart, P S Hart, M D Michalec, et al.
Caries Research|May 26, 2005
Dental caries and microbial acid production in twinsW A Bretz, P M A Corby, T C Hart, et al.
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.
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.
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 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|December 14, 1999
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndromeT C Hart, P S Hart, D W Bowden, et al.
Journal of Medical Genetics|March 4, 2005
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfectaJ-W Kim, J P Simmer, T C Hart, et al.
Clinical Genetics|February 18, 2009
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfectaP S Hart, S Becerik, D Cogulu, et al.
Journal of Medical Genetics|February 9, 2000
Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutationT C Hart, P S Hart, M D Michalec, et al.
Caries Research|May 26, 2005
Dental caries and microbial acid production in twinsW A Bretz, P M A Corby, T C Hart, et al.
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.
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.
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 10