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Journal of Child Neurology
|
April 16, 1998
Cavum septi pellucidi and cavum vergae in normal and developmentally delayed populations
J B Bodensteiner, G B Schaefer, J M Craft
American Journal of Medical Genetics
|
October 1, 1993
Patient with double heterozygosity for achondroplasia and pseudoachondroplasia, with comments on these conditions and the relationship between pseudoachondroplasia and multiple epiphyseal dysplasia, Fairbank type
L O Langer, G B Schaefer, D T Wadsworth
American Journal of Medical Genetics
|
January 20, 1997
Marshall-Stickler phenotype associated with von Willebrand disease
M R MacDonald, K S Baker, G B Schaefer
Journal of Child Neurology
|
January 1, 1994
Hypoplasia of the corpus callosum: a study of 445 consecutive MRI scans
J Bodensteiner, G B Schaefer, L Breeding, et al.
Clinical Biochemistry
|
July 1, 1998
Accelerated linear growth and advanced bone age in Sotos syndrome is not associated with abnormalities of collagen metabolism
V H Rao, B A Buehler, G B Schaefer
Clinics in Communication Disorders
|
January 1, 1992
Neurogenetic aspects of communication disorders
G B Schaefer, P Mathy-Laikko, J B Bodensteiner
Neurologic Clinics
|
November 1, 1994
Cerebral dysgenesis. An overview
G B Schaefer, R D Sheth, J B Bodensteiner
Clinical Genetics
|
February 1, 1997
Clinical variability of tetrasomy 12p
G B Schaefer, A Jochar, R Muneer, et al.
Ear, Nose, & Throat Journal
|
November 5, 1997
Stickler syndrome
M R MacDonald, P Kolodziej, G B Schaefer, et al.
Pediatric Neurology
|
July 1, 1985
Computed tomography and magnetic resonance imaging in late-onset globoid cell leukodystrophy (Krabbe disease)
R D Brownsworth, J B Bodensteiner, G B Schaefer, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 81) with videos related to
Sort By:
Page
of 9
Journal of Child Neurology
|
April 16, 1998
Cavum septi pellucidi and cavum vergae in normal and developmentally delayed populations
J B Bodensteiner, G B Schaefer, J M Craft
American Journal of Medical Genetics
|
October 1, 1993
Patient with double heterozygosity for achondroplasia and pseudoachondroplasia, with comments on these conditions and the relationship between pseudoachondroplasia and multiple epiphyseal dysplasia, Fairbank type
L O Langer, G B Schaefer, D T Wadsworth
American Journal of Medical Genetics
|
January 20, 1997
Marshall-Stickler phenotype associated with von Willebrand disease
M R MacDonald, K S Baker, G B Schaefer
Journal of Child Neurology
|
January 1, 1994
Hypoplasia of the corpus callosum: a study of 445 consecutive MRI scans
J Bodensteiner, G B Schaefer, L Breeding, et al.
Clinical Biochemistry
|
July 1, 1998
Accelerated linear growth and advanced bone age in Sotos syndrome is not associated with abnormalities of collagen metabolism
V H Rao, B A Buehler, G B Schaefer
Clinics in Communication Disorders
|
January 1, 1992
Neurogenetic aspects of communication disorders
G B Schaefer, P Mathy-Laikko, J B Bodensteiner
Neurologic Clinics
|
November 1, 1994
Cerebral dysgenesis. An overview
G B Schaefer, R D Sheth, J B Bodensteiner
Clinical Genetics
|
February 1, 1997
Clinical variability of tetrasomy 12p
G B Schaefer, A Jochar, R Muneer, et al.
Ear, Nose, & Throat Journal
|
November 5, 1997
Stickler syndrome
M R MacDonald, P Kolodziej, G B Schaefer, et al.
Pediatric Neurology
|
July 1, 1985
Computed tomography and magnetic resonance imaging in late-onset globoid cell leukodystrophy (Krabbe disease)
R D Brownsworth, J B Bodensteiner, G B Schaefer, et al.
Page
of 9