Showing results (141-150 of 155) with videos related to
Sort By:
Pageof 16
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1992
Cranial base angulation and prognathism related to cranial and general skeletal maturation in human fetusesB van den Eynde, I Kjaer, B Solow, et al.IEEE Transactions on Medical Imaging|February 24, 2001
Surface-bounded growth modeling applied to human mandiblesP R Andresen, F L Bookstein, K Conradsen, et al.Clinical Genetics|May 31, 2008
X-linked hypohidrotic ectodermal dysplasia. Genetic and dental findings in 67 Danish patients from 19 familiesM O Lexner, A Bardow, I Juncker, et al.Fetal Diagnosis and Therapy|January 27, 2009
Prenatal 3D ultrasound diagnostics in cleidocranial dysplasiaN V Hermann, H D Hove, C Jørgensen, et al.Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|August 1, 1990
Structure and function of masticatory muscles in a case of muscular dystrophyM Bakke, S Kirkeby, B L Jensen, et al.Plastic and Reconstructive Surgery|August 18, 2000
Quantification of osseous facial dysmorphology in untreated unilateral coronal synostosisA A Kane, Y O Kim, A Eaton, et al.Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|July 1, 1993
Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromesS Kreiborg, J L Marsh, M M Cohen, et al.Plastic and Reconstructive Surgery|July 1, 1996
The role of bone centers in the pathogenesis of craniosynostosis: an embryologic approach using CT measurements in isolated craniosynostosis and Apert and Crouzon syndromesI M Mathijssen, J M Vaandrager, J C van der Meulen, et al.American Journal of Medical Genetics. Part A|February 4, 2005
Delineation of an interstitial 9q22 deletion in basal cell nevus syndromeS E Boonen, D Stahl, S Kreiborg, et al.American Journal of Medical Genetics|March 11, 1992
Birth prevalence study of the Apert syndromeM M Cohen, S Kreiborg, E J Lammer, et al.Pageof 16