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Skeletal Radiology|February 1, 1997
Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tardaK W Gripp, C I Scott, L Nicholson, et al.American Journal of Medical Genetics|April 17, 1999
Neuroanatomic and neuropsychological outcome in school-age children with achondroplasiaN M Thompson, J T Hecht, T P Bohan, et al.Nature Genetics|September 1, 1996
The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genesD Stickens, G Clines, D Burbee, et al.European Journal of Pediatrics|December 1, 1986
Foramen magnum stenosis in homozygous achondroplasiaJ T Hecht, W A Horton, I J Butler, et al.The Journal of Rheumatology|April 1, 1993
Inflammatory arthropathies in children with chromosomal abnormalitiesD H Ihnat, G McIlvain-Simpson, K Conard, et al.Developmental Medicine and Child Neurology|January 1, 1994
The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndromeB M Finucane, D Konar, B Haas-Givler, et al.American Journal of Medical Genetics|February 15, 1993
Eye abnormalities in the Smith-Magenis contiguous gene deletion syndromeB M Finucane, E R Jaeger, M B Kurtz, et al.American Journal of Medical Genetics|May 3, 1996
Sponastrime dysplasia: five new cases and review of nine previously published casesL O Langer, R K Beals, S LaFranchi, et al.Annals of Neurology|January 1, 1980
Central core disease and malignant hyperthermia syndromeJ P Frank, Y Harati, I J Butler, et al.American Journal of Medical Genetics|November 11, 1996
Extending the spectrum of distal arthrogryposisK W Gripp, C I Scott, B C Brockett, et al.Pageof 14