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D L Rimoin

Showing results (241-250 of 284) with videos related to

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The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, 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|December 5, 2000
Oto-palato-digital syndrome, type II: report of three cases with further delineation of the chondro-osseous morphologyR Savarirayan, V Cormier-Daire, S Unger, et al.
American Journal of Medical Genetics|July 24, 1998
Molecular, radiologic, and histopathologic correlations in thanatophoric dysplasiaW R Wilcox, P L Tavormina, D Krakow, et al.
American Journal of Medical Genetics|August 26, 1998
Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindredM Ahmad, M Faiyaz Ul Haque, W Ahmad, et al.
Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.
American Journal of Medical Genetics|April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndromeH Chen, L Immken, R Lachman, et al.
Pathology and Immunopathology Research|January 1, 1988
New perspectives in the human chondrodysplasiasW A Horton, P F Goetinck, S M Sayedin, et al.
Prenatal Diagnosis|November 1, 1993
Fetal akinesia/hypokinesia sequence: prenatal diagnosis and intra-familial variabilityC A Bacino, L D Platt, A Garber, et al.
Pageof 29

Showing results (241-250 of 284) with videos related to

Sort By:
Pageof 29
The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, 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|December 5, 2000
Oto-palato-digital syndrome, type II: report of three cases with further delineation of the chondro-osseous morphologyR Savarirayan, V Cormier-Daire, S Unger, et al.
American Journal of Medical Genetics|July 24, 1998
Molecular, radiologic, and histopathologic correlations in thanatophoric dysplasiaW R Wilcox, P L Tavormina, D Krakow, et al.
American Journal of Medical Genetics|August 26, 1998
Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindredM Ahmad, M Faiyaz Ul Haque, W Ahmad, et al.
Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.
American Journal of Medical Genetics|April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndromeH Chen, L Immken, R Lachman, et al.
Pathology and Immunopathology Research|January 1, 1988
New perspectives in the human chondrodysplasiasW A Horton, P F Goetinck, S M Sayedin, et al.
Prenatal Diagnosis|November 1, 1993
Fetal akinesia/hypokinesia sequence: prenatal diagnosis and intra-familial variabilityC A Bacino, L D Platt, A Garber, et al.
Pageof 29