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Progress in Clinical and Biological Research
|
January 1, 1985
The mouse skeletal mutants: models for the human skeletal dysplasias
D J Eteson, D O Sillence, R S Lachman, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 28, 2003
Use of three-dimensional ultrasound imaging in the diagnosis of prenatal-onset skeletal dysplasias
D Krakow, J Williams, M Poehl, et al.
Progress in Clinical and Biological Research
|
January 1, 1984
Genetics, diabetes mellitus heterogeneity, and coronary heart disease
J I Rotter, C M Vadheim, L J Raffel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1990
Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasia
G E Tiller, D L Rimoin, L W Murray, et al.
The Journal of Pediatrics
|
May 1, 1979
Further heterogeneity within lethal neonatal short-limbed dwarfism: the platyspondylic types
W A Horton, D L Rimoin, D W Hollister, et al.
American Journal of Diseases of Children (1960)
|
July 1, 1970
Thanatophoric dwarfism
R L Kaufman, D L Rimoin, W H McAlister, et al.
American Journal of Diseases of Children (1960)
|
January 1, 1974
Variable expression of the Holt-Oram syndrome
R L Kaufman, D L Rimoin, W H McAlister, et al.
American Journal of Optometry and Physiological Optics
|
February 1, 1980
Optometric screening in achondroplasia, diastrophic dysplasia, and spondyloepiphyseal dysplasia congenita
J R Griffin, J E Ault, D O Sillence, et al.
Birth Defects Original Article Series
|
February 1, 1971
An oculocerebrofacial syndrome
R L Kaufman, D L Rimoin, A L Prensky, et al.
The New England Journal of Medicine
|
February 11, 1971
Multiple cell origin of hereditary neurofibromas
P J Fialkow, R W Sagebiel, S M Gartler, et al.
Page
of 29
Search research articles
Search
Showing results (131-140 of 284) with videos related to
Sort By:
Page
of 29
Progress in Clinical and Biological Research
|
January 1, 1985
The mouse skeletal mutants: models for the human skeletal dysplasias
D J Eteson, D O Sillence, R S Lachman, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 28, 2003
Use of three-dimensional ultrasound imaging in the diagnosis of prenatal-onset skeletal dysplasias
D Krakow, J Williams, M Poehl, et al.
Progress in Clinical and Biological Research
|
January 1, 1984
Genetics, diabetes mellitus heterogeneity, and coronary heart disease
J I Rotter, C M Vadheim, L J Raffel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1990
Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasia
G E Tiller, D L Rimoin, L W Murray, et al.
The Journal of Pediatrics
|
May 1, 1979
Further heterogeneity within lethal neonatal short-limbed dwarfism: the platyspondylic types
W A Horton, D L Rimoin, D W Hollister, et al.
American Journal of Diseases of Children (1960)
|
July 1, 1970
Thanatophoric dwarfism
R L Kaufman, D L Rimoin, W H McAlister, et al.
American Journal of Diseases of Children (1960)
|
January 1, 1974
Variable expression of the Holt-Oram syndrome
R L Kaufman, D L Rimoin, W H McAlister, et al.
American Journal of Optometry and Physiological Optics
|
February 1, 1980
Optometric screening in achondroplasia, diastrophic dysplasia, and spondyloepiphyseal dysplasia congenita
J R Griffin, J E Ault, D O Sillence, et al.
Birth Defects Original Article Series
|
February 1, 1971
An oculocerebrofacial syndrome
R L Kaufman, D L Rimoin, A L Prensky, et al.
The New England Journal of Medicine
|
February 11, 1971
Multiple cell origin of hereditary neurofibromas
P J Fialkow, R W Sagebiel, S M Gartler, et al.
Page
of 29