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Genomics|June 14, 2000
Confirmation of the mapping of the Camurati-Englemann locus to 19q13. 2 and refinement to a 3.2-cM regionS P Vaughn, S Broussard, C R Hall, et al.Genomics|November 26, 1998
Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palateK Yoshiura, J Machida, S Daack-Hirsch, et al.Journal of Pediatric Surgery|December 1, 1995
3-Year-old phenotypic female with campomelic dysplasia and bilateral gonadoblastomaJ R Hong, M Barber, C I Scott, et al.American Journal of Medical Genetics|November 1, 1984
Reproduction in XYY males: two new cases and implications for genetic counselingF Grass, J McCombs, C I Scott, et al.Journal of Medical Genetics|September 11, 1998
Medical complications of achondroplasia: a multicentre patient reviewA G Hunter, A Bankier, J G Rogers, et al.Skeletal Radiology|January 1, 1989
Scintigraphic differentiation of congenital soft-tissue extremity enlargement with Tc-99m DTPAG A Mandell, C I Scott, H T Harcke, et al.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.Journal of Applied Physiology (Bethesda, Md. : 1985)|November 1, 1990
Proton magnetic resonance of exercise-induced water changes in gastrocnemius muscleL K Fotedar, J M Slopis, P A Narayana, 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.Pageof 21