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C I Scott

Showing results (101-110 of 116) with videos related to

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Skeletal Radiology|January 1, 1989
Identification of avascular necrosis in the dysplastic proximal femoral epiphysisG A Mandell, W G MacKenzie, C I Scott, et al.
Birth Defects Original Article Series|January 1, 1975
Difficulties in the classification of the epiphyseal dysplasiasR S Lachman, D L Rimoin, J G Hall, et al.
Birth Defects Original Article Series|January 1, 1977
Grebe chondrodysplasia and similar forms of severe short-limbed dwarfismG Romeo, J Zonana, R S Lachman, et al.
American Journal of Medical Genetics|January 1, 1981
Comments on the Neu-Laxova syndrome and CAD complexC I Scott, J M Louro, K M Laurence, et al.
American Journal of Medical Genetics|November 20, 1995
Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patientR C Juyal, B Finucane, L G Shaffer, et al.
The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.
The Journal of Pediatrics|October 1, 1978
The phenotypic variability of diastrophic dysplasiaW A Horton, D L Rimoin, R S Lachman, et al.
American Journal of Medical Genetics|January 1, 1977
Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: mucopolysacchariodosis IVBA I Arbisser, K A Donnelly, C I Scott, et al.
American Journal of Human Genetics|November 1, 1981
The Sabinas syndromeR R Howell, A I Arbisser, D S Parsons, et al.
American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.
Pageof 12

Showing results (101-110 of 116) with videos related to

Sort By:
Pageof 12
Skeletal Radiology|January 1, 1989
Identification of avascular necrosis in the dysplastic proximal femoral epiphysisG A Mandell, W G MacKenzie, C I Scott, et al.
Birth Defects Original Article Series|January 1, 1975
Difficulties in the classification of the epiphyseal dysplasiasR S Lachman, D L Rimoin, J G Hall, et al.
Birth Defects Original Article Series|January 1, 1977
Grebe chondrodysplasia and similar forms of severe short-limbed dwarfismG Romeo, J Zonana, R S Lachman, et al.
American Journal of Medical Genetics|January 1, 1981
Comments on the Neu-Laxova syndrome and CAD complexC I Scott, J M Louro, K M Laurence, et al.
American Journal of Medical Genetics|November 20, 1995
Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patientR C Juyal, B Finucane, L G Shaffer, et al.
The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.
The Journal of Pediatrics|October 1, 1978
The phenotypic variability of diastrophic dysplasiaW A Horton, D L Rimoin, R S Lachman, et al.
American Journal of Medical Genetics|January 1, 1977
Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: mucopolysacchariodosis IVBA I Arbisser, K A Donnelly, C I Scott, et al.
American Journal of Human Genetics|November 1, 1981
The Sabinas syndromeR R Howell, A I Arbisser, D S Parsons, et al.
American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.
Pageof 12