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Journal of Medical Genetics|December 1, 1988
A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical featuresJ Christodoulou, R K Hall, S Menahem, et al.The Biochemical Journal|December 15, 1986
Collagen defects in lethal perinatal osteogenesis imperfectaJ F Bateman, D Chan, T Mascara, et al.Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.The Journal of Bone and Joint Surgery. British Volume|November 1, 1990
Development of the hip in multiple epiphyseal dysplasia. Natural history and susceptibility to premature osteoarthritisN J Treble, F O Jensen, A Bankier, et al.The Journal of Biological Chemistry|May 25, 1987
Lethal perinatal osteogenesis imperfecta due to the substitution of arginine for glycine at residue 391 of the alpha 1(I) chain of type I collagenJ F Bateman, D Chan, I D Walker, et al.Journal of Medical Genetics|November 1, 1996
Disrupted growth plates and progressive deformities in osteogenesis imperfecta as a result of the substitution of glycine 585 by valine in the alpha 2 (I) chain of type I collagenW G Cole, D Chan, C W Chow, et al.American Journal of Medical Genetics|December 2, 1996
Pitt-Rogers-Danks syndrome: the result of a 4p microdeletionM Clemens, J T Martsolf, J G Rogers, et al.Acta Neuropathologica|January 1, 1988
Neuropathology in glutaric acidaemia type 1C W Chow, E A Haan, S I Goodman, et al.American Journal of Medical Genetics|January 1, 1981
Further delineation of the C (trigonocephaly) syndromeR M Antley, D S Hwang, W Theopold, et al.JDR Clinical and Translational Research|April 3, 2019
Reducing Potentially Preventable Dental Hospitalizations of Young Children: A Community-Level AnalysisJ G Rogers, G G Adams, F A C Wright, et al.Pageof 19