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American Journal of Medical Genetics|January 1, 1980
The G syndrome--additional observationsS Arya, C Viseskul, E F GilbertArchives of Pathology & Laboratory Medicine|April 1, 1983
Leigh's necrotizing encephalopathy with pyruvate carboxylase deficiencyE F Gilbert, S Arya, R ChunAmerican Journal of Diseases of Children (1960)|April 1, 1982
Growth curves for height for diastrophic dysplasia, spondyloepiphyseal dysplasia congenita, and pseudoachondroplasiaW A Horton, J G Hall, C I Scott, et al.The Journal of Pediatrics|December 1, 1983
A distinct chondrodysplasia resembling Kniest dysplasia: clinical, roentgenographic, histologic, and ultrastructural findingsS M Sconyers, D L Rimoin, R S Lachman, et al.American Journal of Medical Genetics|January 9, 2001
Scapuloiliac dysostosis (Kosenow syndrome, pelvis-shoulder dysplasia) spectrum: three additional casesA M Elliott, E R Roeder, D R Witt, et al.American Journal of Medical Genetics|February 1, 1984
Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneityD O Sillence, K K Barlow, A P Garber, et al.The Journal of Pediatrics|September 1, 1978
Standard growth curves for achondroplasiaW A Horton, J I Rotter, D L Rimoin, et al.Prenatal Diagnosis|January 1, 1987
Prenatal diagnosis of osteogenesis imperfecta type IIIL P Robinson, N J Worthen, R S Lachman, et al.Clinical Science (London, England : 1979)|July 31, 1998
Neutrophil priming: pathophysiological consequences and underlying mechanismsA M Condliffe, E Kitchen, E R ChilversAmerican Journal of Medical Genetics|February 1, 1993
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathologyZ Borochowitz, L O Langer, H E Gruber, et al.Pageof 59