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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 update
R 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 syndrome
V J Rappaport, T Falik-Borenstein, R D Clark, et al.
Annals of Internal Medicine
|
April 1, 1986
New frontiers in genetic medicine
L 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 chondrodysplasia
H E Gruber, C R Greenberg, R S Lachman, et al.
Birth Defects Original Article Series
|
January 1, 1976
Allelic mutations in the mucopolysaccharidoses
J Leisti, D L Rimoin, M Kaback, et al.
Birth Defects Original Article Series
|
January 1, 1975
Craniodiaphyseal dysplasia
I 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 gestation
M 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 mucopolysaccharidosis
W 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 fetuses
M D Levine, R Lachman, D L Rimoin, et al.
Pediatric Radiology
|
February 9, 2000
Pathological fractures in spondyloenchondrodysplasia: case report
Y Udler, G J Halpern, R S Lachman, et al.
Page
of 29
Search research articles
Search
Showing results (141-150 of 284) with videos related to
Sort By:
Page
of 29
European Journal of Radiology
|
January 11, 1992
Collagen, genes and the skeletal dysplasias on the edge of a new era: a review and update
R 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 syndrome
V J Rappaport, T Falik-Borenstein, R D Clark, et al.
Annals of Internal Medicine
|
April 1, 1986
New frontiers in genetic medicine
L 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 chondrodysplasia
H E Gruber, C R Greenberg, R S Lachman, et al.
Birth Defects Original Article Series
|
January 1, 1976
Allelic mutations in the mucopolysaccharidoses
J Leisti, D L Rimoin, M Kaback, et al.
Birth Defects Original Article Series
|
January 1, 1975
Craniodiaphyseal dysplasia
I 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 gestation
M 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 mucopolysaccharidosis
W 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 fetuses
M D Levine, R Lachman, D L Rimoin, et al.
Pediatric Radiology
|
February 9, 2000
Pathological fractures in spondyloenchondrodysplasia: case report
Y Udler, G J Halpern, R S Lachman, et al.
Page
of 29