Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C I Scott

Showing results (21-30 of 116) with videos related to

Pageof 12
Sort By:
Journal of Medical Genetics|October 11, 1976
Discordance for Cornelia de Lange syndrome in twinsR E Stevenson, C I Scott
Clinical Genetics|September 1, 1981
Recurrent unilateral hand malformations in siblingsJ T Hecht, C I Scott
Pediatric Clinics of North America|February 1, 1973
Genetic disorders associated with mental retardation. Clinical aspectsC I Scott, G H Thomas
Birth Defects Original Article Series|June 1, 1971
Focal dermal hypoplasia (Goltz syndrome): a follow-upC I Scott, F G Moyer
Clinical Genetics|December 1, 1981
Limb deficiency syndrome in half-sibsJ T Hecht, C I Scott
Clinical Genetics|January 1, 1984
The Schinzel syndrome in a mother and daughterJ T Hecht, C I Scott
American Journal of Medical Genetics|June 13, 1997
Extended survival in a new case of ter Haar syndrome: further delineation of the syndromeR Wallerstein, C I Scott, L Nicholson
Clinical Orthopaedics and Related Research|January 11, 2000
Involvement of the humerus in two generations with spondyloepiphyseal dysplasiaU Givon, S J Kumar, C I Scott
The Johns Hopkins Medical Journal|May 1, 1971
An infant with 45 chromosomes including a D-E (13-15-17-18) translocation chromosomeD S Borgaonkar, E Mules, C I Scott
Clinical Dysmorphology|October 1, 1996
Bilateral duplication of the primary ulnar ossification center in Ellis-van Creveld syndromeK W Gripp, C I Scott, L Nicholson
Pageof 12

Showing results (21-30 of 116) with videos related to

Sort By:
Pageof 12
Journal of Medical Genetics|October 11, 1976
Discordance for Cornelia de Lange syndrome in twinsR E Stevenson, C I Scott
Clinical Genetics|September 1, 1981
Recurrent unilateral hand malformations in siblingsJ T Hecht, C I Scott
Pediatric Clinics of North America|February 1, 1973
Genetic disorders associated with mental retardation. Clinical aspectsC I Scott, G H Thomas
Birth Defects Original Article Series|June 1, 1971
Focal dermal hypoplasia (Goltz syndrome): a follow-upC I Scott, F G Moyer
Clinical Genetics|December 1, 1981
Limb deficiency syndrome in half-sibsJ T Hecht, C I Scott
Clinical Genetics|January 1, 1984
The Schinzel syndrome in a mother and daughterJ T Hecht, C I Scott
American Journal of Medical Genetics|June 13, 1997
Extended survival in a new case of ter Haar syndrome: further delineation of the syndromeR Wallerstein, C I Scott, L Nicholson
Clinical Orthopaedics and Related Research|January 11, 2000
Involvement of the humerus in two generations with spondyloepiphyseal dysplasiaU Givon, S J Kumar, C I Scott
The Johns Hopkins Medical Journal|May 1, 1971
An infant with 45 chromosomes including a D-E (13-15-17-18) translocation chromosomeD S Borgaonkar, E Mules, C I Scott
Clinical Dysmorphology|October 1, 1996
Bilateral duplication of the primary ulnar ossification center in Ellis-van Creveld syndromeK W Gripp, C I Scott, L Nicholson
Pageof 12