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Clinical Oral Implants Research|February 13, 2001
Prosthetic management of the partially dentate patient with fixed implant restorationsU C Belser, R Mericske-Stern, J P Bernard, et al.
The Journal of Prosthetic Dentistry|November 1, 1984
Prosthodontic survey. Part II: Removable prosthodontic curriculum surveyT D Taylor, S A Aquilino, A C Matthews, et al.
The International Journal of Oral & Maxillofacial Implants|January 5, 2002
Retentiveness of dental cements used with metallic implant componentsR S Squier, J R Agar, J P Duncan, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|July 25, 2000
A novel gene, DSCR5, from the distal Down syndrome critical region on chromosome 21q22.2T Togashi, D K Choi, T D Taylor, et al.
The Journal of Investigative Dermatology|July 17, 1998
Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with evidence for multiple independent mutationsT D Taylor, S J Hayflick, W McKinnon, et al.
Annals of Plastic Surgery|May 1, 1996
Total midface reconstruction after radical tumor resection: a case report and overview of the problemG P Reece, J C Lemon, R F Jacob, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 2, 2001
Molecular cloning and characterization of a gene expressed in mouse developing tongue, mDscr5 gene, a homolog of human DSCR5 (Down syndrome Critical Region gene 5)D K Choi, Y Suzuki, S Yoshimura, et al.
Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons|October 1, 1988
Collagen/hydroxylapatite implant for augmenting deficient alveolar ridges: twelve-month clinical dataD R Mehlisch, T D Taylor, D G Leibold, et al.
Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons|May 1, 1987
Evaluation of collagen/hydroxylapatite for augmenting deficient alveolar ridges: a preliminary reportD R Mehlisch, T D Taylor, D G Leibold, et al.
Nature Genetics|December 1, 1996
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13T D Taylor, M Litt, P Kramer, et al.
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