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Journal of Medical Genetics|February 9, 1999
De novo 10q22 interstitial deletionL Cook, D D Weaver, J K Hartsfield, et al.Clinical Genetics|July 11, 1998
Partners with reciprocal translocations: genetic counseling for the 'double translocation'L Cook, J K Hartsfield, G H VanceJournal of Medical Genetics|June 4, 1998
49,XXXXY: a distinct phenotype. Three new cases and reviewJ Peet, D D Weaver, G H VanceAmerican Journal of Medical Genetics|February 27, 2001
Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implicationsL E Walsh, G H Vance, D D WeaverOrthodontics & Craniofacial Research|July 25, 2009
Pathways in external apical root resorption associated with orthodontiaJ K HartsfieldAdvances in Pediatrics|January 1, 1994
Premature exfoliation of teeth in childhood and adolescenceJ K HartsfieldOrthodontics & Craniofacial Research|July 27, 2007
Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia)J K HartsfieldAmerican Journal of Medical Genetics|October 22, 1998
Weaver syndrome: autosomal dominant inheritance of the disorderV K Proud, S R Braddock, L Cook, et al.American Journal of Medical Genetics|February 7, 1998
Urorectal septum malformation sequence: report of thirteen additional cases and review of the literatureP G Wheeler, D D Weaver, M O Obeime, et al.Oral Surgery, Oral Medicine, and Oral Pathology|June 1, 1984
Bilateral macrostomia in one of monozygotic twinsJ K Hartsfield, D BixlerPageof 250