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D L Rimoin

Showing results (91-100 of 284) with videos related to

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Lancet (London, England)|May 19, 1984
Inheritance of immunoglobulin light-chain genes in pairs of siblings with insulin-dependent diabetes mellitusL L Field, C E Anderson, D L Rimoin
Birth Defects Original Article Series|January 1, 1974
Type C brachydactyly with limited flexion of distal interphalangeal jointsD L Rimoin, D W Hollister, R S Lachman
American Journal of Human Genetics|January 1, 1973
Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromesR J Warren, D L Rimoin, R L Summitt
American Journal of Medical Genetics|June 1, 1986
Achondrogenesis II-hypochondrogenesis: variability versus heterogeneityZ Borochowitz, A Ornoy, R Lachman, et al.
Pathology and Immunopathology Research|January 1, 1988
Comparisons and correlations of skeletal defects in mouse and humanD L Rimoin, D J Eteson, D O Sillence
Scanning Microscopy|September 1, 1990
Calcospherite (calcification nodule) size in the short rib polydactyly syndromesH E Gruber, R S Lachman, D L Rimoin
The American Journal of Pathology|September 1, 1979
Morphologic studies in the skeletal dysplasiasD O Sillence, W A Horton, D L Rimoin
Lancet (London, England)|May 19, 1979
Genetic heterogeneity in peptic ulcerJ I Rotter, D L Rimoin, I M Samloff
Pediatric Radiology|May 1, 1997
The scapula as a window to the diagnosis of skeletal dysplasiasG R Mortier, D L Rimoin, R S Lachman
The Journal of Pediatrics|September 1, 1987
Fetal varicella syndromeA L Alkalay, J J Pomerance, D L Rimoin
Pageof 29

Showing results (91-100 of 284) with videos related to

Sort By:
Pageof 29
Lancet (London, England)|May 19, 1984
Inheritance of immunoglobulin light-chain genes in pairs of siblings with insulin-dependent diabetes mellitusL L Field, C E Anderson, D L Rimoin
Birth Defects Original Article Series|January 1, 1974
Type C brachydactyly with limited flexion of distal interphalangeal jointsD L Rimoin, D W Hollister, R S Lachman
American Journal of Human Genetics|January 1, 1973
Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromesR J Warren, D L Rimoin, R L Summitt
American Journal of Medical Genetics|June 1, 1986
Achondrogenesis II-hypochondrogenesis: variability versus heterogeneityZ Borochowitz, A Ornoy, R Lachman, et al.
Pathology and Immunopathology Research|January 1, 1988
Comparisons and correlations of skeletal defects in mouse and humanD L Rimoin, D J Eteson, D O Sillence
Scanning Microscopy|September 1, 1990
Calcospherite (calcification nodule) size in the short rib polydactyly syndromesH E Gruber, R S Lachman, D L Rimoin
The American Journal of Pathology|September 1, 1979
Morphologic studies in the skeletal dysplasiasD O Sillence, W A Horton, D L Rimoin
Lancet (London, England)|May 19, 1979
Genetic heterogeneity in peptic ulcerJ I Rotter, D L Rimoin, I M Samloff
Pediatric Radiology|May 1, 1997
The scapula as a window to the diagnosis of skeletal dysplasiasG R Mortier, D L Rimoin, R S Lachman
The Journal of Pediatrics|September 1, 1987
Fetal varicella syndromeA L Alkalay, J J Pomerance, D L Rimoin
Pageof 29