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D L Rimoin

Showing results (141-150 of 284) with videos related to

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European Journal of Radiology|January 11, 1992
Collagen, genes and the skeletal dysplasias on the edge of a new era: a review and updateR S Lachman, G E Tiller, J M Graham, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|June 1, 1989
Neonatal genetic casebook. The de Lange syndromeV J Rappaport, T Falik-Borenstein, R D Clark, et al.
Annals of Internal Medicine|April 1, 1986
New frontiers in genetic medicineL J Shapiro, D E Comings, O W Jones, et al.
Ultrastructural Pathology|July 1, 1990
Ultrastructural abnormalities in bone and calcifying cartilage in two siblings with a newly described recessive lethal chondrodysplasiaH E Gruber, C R Greenberg, R S Lachman, et al.
Birth Defects Original Article Series|January 1, 1976
Allelic mutations in the mucopolysaccharidosesJ Leisti, D L Rimoin, M Kaback, et al.
Birth Defects Original Article Series|January 1, 1975
Craniodiaphyseal dysplasiaI Kaitila, R E Stewart, E Landow, et al.
AJR. American Journal of Roentgenology|January 1, 1991
Normal sonographic appearance of a thanatophoric dwarf variant fetus at 13 weeks gestationM B Macken, E B Grantmyre, D L Rimoin, et al.
The Journal of Pediatrics|February 1, 1973
Beta glucuronidase deficiency: report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosisW S Sly, B A Quinton, W H McAlister, et al.
Birth Defects Original Article Series|January 1, 1975
Diagnosis of skeletal dysplasias in second trimester fetusesM D Levine, R Lachman, D L Rimoin, et al.
Pediatric Radiology|February 9, 2000
Pathological fractures in spondyloenchondrodysplasia: case reportY Udler, G J Halpern, R S Lachman, et al.
Pageof 29

Showing results (141-150 of 284) with videos related to

Sort By:
Pageof 29
European Journal of Radiology|January 11, 1992
Collagen, genes and the skeletal dysplasias on the edge of a new era: a review and updateR S Lachman, G E Tiller, J M Graham, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|June 1, 1989
Neonatal genetic casebook. The de Lange syndromeV J Rappaport, T Falik-Borenstein, R D Clark, et al.
Annals of Internal Medicine|April 1, 1986
New frontiers in genetic medicineL J Shapiro, D E Comings, O W Jones, et al.
Ultrastructural Pathology|July 1, 1990
Ultrastructural abnormalities in bone and calcifying cartilage in two siblings with a newly described recessive lethal chondrodysplasiaH E Gruber, C R Greenberg, R S Lachman, et al.
Birth Defects Original Article Series|January 1, 1976
Allelic mutations in the mucopolysaccharidosesJ Leisti, D L Rimoin, M Kaback, et al.
Birth Defects Original Article Series|January 1, 1975
Craniodiaphyseal dysplasiaI Kaitila, R E Stewart, E Landow, et al.
AJR. American Journal of Roentgenology|January 1, 1991
Normal sonographic appearance of a thanatophoric dwarf variant fetus at 13 weeks gestationM B Macken, E B Grantmyre, D L Rimoin, et al.
The Journal of Pediatrics|February 1, 1973
Beta glucuronidase deficiency: report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosisW S Sly, B A Quinton, W H McAlister, et al.
Birth Defects Original Article Series|January 1, 1975
Diagnosis of skeletal dysplasias in second trimester fetusesM D Levine, R Lachman, D L Rimoin, et al.
Pediatric Radiology|February 9, 2000
Pathological fractures in spondyloenchondrodysplasia: case reportY Udler, G J Halpern, R S Lachman, et al.
Pageof 29