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Journal of Periodontology
|
March 1, 1992
Re-interpretation of the evidence for X-linked dominant inheritance of juvenile periodontitis
T C Hart, M L Marazita, H A Schenkein, et al.
Spatial and Spatio-Temporal Epidemiology
|
April 4, 2012
Error propagation models to examine the effects of geocoding quality on spatial analysis of individual-level datasets
P A Zandbergen, T C Hart, K E Lenzer, et al.
Human Mutation
|
November 3, 2000
Two 3' polymorphisms in DLX5: g126427delTATC and g126249T-->C
P S Hart, M D Michalec, J T Wright, et al.
Human Mutation
|
February 19, 2000
Polymorphism (g2035C>T) in the amelogenin gene
P S Hart, A C Vlaservich, T C Hart, et al.
The Journal of Clinical Pediatric Dentistry
|
January 1, 1992
Comparison of dentofacial morphology in monozygotic twin pairs with their siblings using LISREL
T C Ramsey, M S Sorin, T C Hart, et al.
Archives of Oral Biology
|
April 2, 2002
A nomenclature for X-linked amelogenesis imperfecta
P S Hart, T C Hart, J P Simmer, et al.
Cytogenetics and Cell Genetics
|
March 11, 1999
Reassignment of peptidyl prolyl isomerase-like 1 gene (PPIL1) to human chromosome region 6p21.1 by radiation hybrid mapping and fluorescence in situ hybridization
S S Mann, M J Pettenati, C von Kap-herr, et al.
Journal of Dental Research
|
October 26, 2006
Characterization of fibroblasts with Son of Sevenless-1 mutation
E J Lee, S I Jang, D Pallos, et al.
American Journal of Medical Genetics
|
October 23, 1997
Analysis of the tricho-dento-osseous syndrome genotype and phenotype
J T Wright, K Kula, K Hall, et al.
Journal of Medical Genetics
|
October 23, 1998
A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families
J A Price, J T Wright, K Kula, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 92) with videos related to
Sort By:
Page
of 10
Journal of Periodontology
|
March 1, 1992
Re-interpretation of the evidence for X-linked dominant inheritance of juvenile periodontitis
T C Hart, M L Marazita, H A Schenkein, et al.
Spatial and Spatio-Temporal Epidemiology
|
April 4, 2012
Error propagation models to examine the effects of geocoding quality on spatial analysis of individual-level datasets
P A Zandbergen, T C Hart, K E Lenzer, et al.
Human Mutation
|
November 3, 2000
Two 3' polymorphisms in DLX5: g126427delTATC and g126249T-->C
P S Hart, M D Michalec, J T Wright, et al.
Human Mutation
|
February 19, 2000
Polymorphism (g2035C>T) in the amelogenin gene
P S Hart, A C Vlaservich, T C Hart, et al.
The Journal of Clinical Pediatric Dentistry
|
January 1, 1992
Comparison of dentofacial morphology in monozygotic twin pairs with their siblings using LISREL
T C Ramsey, M S Sorin, T C Hart, et al.
Archives of Oral Biology
|
April 2, 2002
A nomenclature for X-linked amelogenesis imperfecta
P S Hart, T C Hart, J P Simmer, et al.
Cytogenetics and Cell Genetics
|
March 11, 1999
Reassignment of peptidyl prolyl isomerase-like 1 gene (PPIL1) to human chromosome region 6p21.1 by radiation hybrid mapping and fluorescence in situ hybridization
S S Mann, M J Pettenati, C von Kap-herr, et al.
Journal of Dental Research
|
October 26, 2006
Characterization of fibroblasts with Son of Sevenless-1 mutation
E J Lee, S I Jang, D Pallos, et al.
American Journal of Medical Genetics
|
October 23, 1997
Analysis of the tricho-dento-osseous syndrome genotype and phenotype
J T Wright, K Kula, K Hall, et al.
Journal of Medical Genetics
|
October 23, 1998
A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families
J A Price, J T Wright, K Kula, et al.
Page
of 10