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D L Rimoin

Showing results (151-160 of 284) with videos related to

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Birth Defects Original Article Series|January 1, 1982
Postmortem findings in the Hurler-Scheie syndrome (mucopolysaccharidosis I-H/S)E R Wassman, K Johnson, L J Shapiro, et al.
Skeletal Radiology|January 1, 1991
Case report 655: Congenital glenoid dysplasia (congenital hypoplasia of the glenoid neck and fossa of the scapula, with accompanied deformity of humeral head, coracoid process, and acromion)Z C Borenstein, J Mink, W Oppenheim, et al.
Pediatric Radiology|February 24, 2001
"Duplicate calcaneus": a rare developmental defect observed in several skeletal dysplasiasV Cormier-Daire, R Savarirayan, S Unger, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Exclusion of the Ellis-van Creveld region on chromosome 4p16 in some families with asphyxiating thoracic dystrophy and short-rib polydactyly syndromesD Krakow, D Salazar, W R Wilcox, et al.
Birth Defects Original Article Series|January 1, 1975
DysosteosclerosisJ Leisti, I Kaitila, R S Lachman, et al.
American Journal of Medical Genetics|April 29, 1998
Lethal syndrome of skeletal dysplasia and progressive central nervous system degenerationM Khosravi, D D Weaver, M J Bull, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1996
Short-term recombinant human growth hormone treatment increases growth rate in achondroplasiaM Shohat, D Tick, S Barakat, et al.
Plastic and Reconstructive Surgery|March 1, 1981
Familial lymphedema praecox: Meige's diseaseE S Wheeler, V Chan, R Wassman, et al.
The American Journal of Pathology|July 1, 1985
Pathologic findings in adenosine deaminase-deficient severe combined immunodeficiency. I. Kidney, adrenal, and chondro-osseous tissue alterationsH Ratech, M A Greco, G Gallo, et al.
American Journal of Human Genetics|November 1, 1983
The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneityS E Hodge, C E Anderson, K Neiswanger, et al.
Pageof 29

Showing results (151-160 of 284) with videos related to

Sort By:
Pageof 29
Birth Defects Original Article Series|January 1, 1982
Postmortem findings in the Hurler-Scheie syndrome (mucopolysaccharidosis I-H/S)E R Wassman, K Johnson, L J Shapiro, et al.
Skeletal Radiology|January 1, 1991
Case report 655: Congenital glenoid dysplasia (congenital hypoplasia of the glenoid neck and fossa of the scapula, with accompanied deformity of humeral head, coracoid process, and acromion)Z C Borenstein, J Mink, W Oppenheim, et al.
Pediatric Radiology|February 24, 2001
"Duplicate calcaneus": a rare developmental defect observed in several skeletal dysplasiasV Cormier-Daire, R Savarirayan, S Unger, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Exclusion of the Ellis-van Creveld region on chromosome 4p16 in some families with asphyxiating thoracic dystrophy and short-rib polydactyly syndromesD Krakow, D Salazar, W R Wilcox, et al.
Birth Defects Original Article Series|January 1, 1975
DysosteosclerosisJ Leisti, I Kaitila, R S Lachman, et al.
American Journal of Medical Genetics|April 29, 1998
Lethal syndrome of skeletal dysplasia and progressive central nervous system degenerationM Khosravi, D D Weaver, M J Bull, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1996
Short-term recombinant human growth hormone treatment increases growth rate in achondroplasiaM Shohat, D Tick, S Barakat, et al.
Plastic and Reconstructive Surgery|March 1, 1981
Familial lymphedema praecox: Meige's diseaseE S Wheeler, V Chan, R Wassman, et al.
The American Journal of Pathology|July 1, 1985
Pathologic findings in adenosine deaminase-deficient severe combined immunodeficiency. I. Kidney, adrenal, and chondro-osseous tissue alterationsH Ratech, M A Greco, G Gallo, et al.
American Journal of Human Genetics|November 1, 1983
The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneityS E Hodge, C E Anderson, K Neiswanger, et al.
Pageof 29