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Archives of Oral Biology
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April 2, 2002
Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations
P S Hart, M J Aldred, P J M Crawford, et al.
Journal of Periodontology
|
June 29, 2000
Genetic polymorphisms of the IL-1alpha and IL-1beta genes in African-American LJP patients and an African-American control population
S J Walker, T E Van Dyke, S Rich, et al.
Journal of Dental Research
|
November 15, 2000
Evidence of genetic heterogeneity for hereditary gingival fibromatosis
T C Hart, D Pallos, L Bozzo, et al.
Journal of Dental Research
|
September 27, 2000
Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation
D B Ravassipour, P S Hart, T C Hart, et al.
Histology and Histopathology
|
June 7, 2003
Characterization and mRNA expression in an unusual odontogenic lesion in a patient with tricho-dento-osseous syndrome
A P Dodds, S A Cox, C A Suggs, et al.
Journal of Medical Genetics
|
July 6, 2004
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
P S Hart, T C Hart, M D Michalec, et al.
Journal of Periodontal Research
|
January 1, 1997
Genetic studies of syndromes with severe periodontitis and palmoplantar hyperkeratosis
T C Hart, A Stabholz, J Meyle, et al.
Oral Diseases
|
January 5, 2008
Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome
D L Domingo, A F Freeman, J Davis, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 21, 2000
An integrated physical and genetic map of the PLS locus interval on chromosome 11q14
T C Hart, S J Walker, D W Bowden, et al.
Journal of Medical Genetics
|
October 3, 1999
Genetic heterogeneity of gingival fibromatosis on chromosome 2p
V Shashi, D Pallos, M J Pettenati, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 92) with videos related to
Sort By:
Page
of 10
Archives of Oral Biology
|
April 2, 2002
Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations
P S Hart, M J Aldred, P J M Crawford, et al.
Journal of Periodontology
|
June 29, 2000
Genetic polymorphisms of the IL-1alpha and IL-1beta genes in African-American LJP patients and an African-American control population
S J Walker, T E Van Dyke, S Rich, et al.
Journal of Dental Research
|
November 15, 2000
Evidence of genetic heterogeneity for hereditary gingival fibromatosis
T C Hart, D Pallos, L Bozzo, et al.
Journal of Dental Research
|
September 27, 2000
Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation
D B Ravassipour, P S Hart, T C Hart, et al.
Histology and Histopathology
|
June 7, 2003
Characterization and mRNA expression in an unusual odontogenic lesion in a patient with tricho-dento-osseous syndrome
A P Dodds, S A Cox, C A Suggs, et al.
Journal of Medical Genetics
|
July 6, 2004
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
P S Hart, T C Hart, M D Michalec, et al.
Journal of Periodontal Research
|
January 1, 1997
Genetic studies of syndromes with severe periodontitis and palmoplantar hyperkeratosis
T C Hart, A Stabholz, J Meyle, et al.
Oral Diseases
|
January 5, 2008
Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome
D L Domingo, A F Freeman, J Davis, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 21, 2000
An integrated physical and genetic map of the PLS locus interval on chromosome 11q14
T C Hart, S J Walker, D W Bowden, et al.
Journal of Medical Genetics
|
October 3, 1999
Genetic heterogeneity of gingival fibromatosis on chromosome 2p
V Shashi, D Pallos, M J Pettenati, et al.
Page
of 10