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C I Scott

Showing results (71-80 of 116) with videos related to

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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.
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.
Humangenetik|January 1, 1973
Identification of a D-E(15-18) translocation chromosome by quinacrine fluorescence and urea banding techniquesD S Borgaonkar, L Ebenezer, C I Scott, et al.
American Journal of Medical Genetics|August 1, 1987
The Nager syndromeJ T Hecht, L L Immken, L F Harris, 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.
American Journal of Medical Genetics. Part A|September 4, 2007
Weight for age charts for children with achondroplasiaJ E Hoover-Fong, J McGready, K J Schulze, et al.
Pageof 12

Showing results (71-80 of 116) with videos related to

Sort By:
Pageof 12
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.
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.
Humangenetik|January 1, 1973
Identification of a D-E(15-18) translocation chromosome by quinacrine fluorescence and urea banding techniquesD S Borgaonkar, L Ebenezer, C I Scott, et al.
American Journal of Medical Genetics|August 1, 1987
The Nager syndromeJ T Hecht, L L Immken, L F Harris, 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.
American Journal of Medical Genetics. Part A|September 4, 2007
Weight for age charts for children with achondroplasiaJ E Hoover-Fong, J McGready, K J Schulze, et al.
Pageof 12