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Pediatric Radiology
|
January 1, 1985
Narrow trachea in mucopolysaccharidoses
M E Peters, S Arya, L O Langer, et al.
American Journal of Medical Genetics
|
February 1, 1993
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology
Z Borochowitz, L O Langer, H E Gruber, et al.
European Journal of Pediatrics
|
August 1, 1980
A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic mother
H J Bruyere, C Viseskul, J M Opitz, et al.
European Journal of Pediatrics
|
May 22, 1978
Spondylocostal dysostosis and urinary tract anomaly: definition and review of an entity
E A Devos, J G Leroy, J J Braeckman, et al.
Birth Defects Original Article Series
|
January 1, 1974
The W syndrome. Studies of malformation syndromes of man XXVIII
P D Pallister, J Herrmann, J W Spranger, et al.
European Journal of Pediatrics
|
August 16, 1976
A severe infantile micromelic chondrodysplasia which resembles Kniest disease
L O Langer, M Gonzalez-Ramos, H Chen, et al.
Pediatric Radiology
|
January 1, 1982
Congenital generalized fibromatosis. Case report and literature review
P W Brill, D R Yandow, L O Langer, et al.
American Journal of Human Genetics
|
March 1, 1995
Genetic heterogeneity in multiple epiphyseal dysplasia
M Deere, S H Blanton, C I Scott, et al.
European Journal of Pediatrics
|
September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infants
E F Gilbert, J M Opitz, J W Spranger, et al.
Skeletal Radiology
|
January 1, 1991
Radiographic features of craniometadiaphyseal dysplasia, wormian bone type
L O Langer, P W Brill, E Afshani, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 61) with videos related to
Sort By:
Page
of 7
Pediatric Radiology
|
January 1, 1985
Narrow trachea in mucopolysaccharidoses
M E Peters, S Arya, L O Langer, et al.
American Journal of Medical Genetics
|
February 1, 1993
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology
Z Borochowitz, L O Langer, H E Gruber, et al.
European Journal of Pediatrics
|
August 1, 1980
A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic mother
H J Bruyere, C Viseskul, J M Opitz, et al.
European Journal of Pediatrics
|
May 22, 1978
Spondylocostal dysostosis and urinary tract anomaly: definition and review of an entity
E A Devos, J G Leroy, J J Braeckman, et al.
Birth Defects Original Article Series
|
January 1, 1974
The W syndrome. Studies of malformation syndromes of man XXVIII
P D Pallister, J Herrmann, J W Spranger, et al.
European Journal of Pediatrics
|
August 16, 1976
A severe infantile micromelic chondrodysplasia which resembles Kniest disease
L O Langer, M Gonzalez-Ramos, H Chen, et al.
Pediatric Radiology
|
January 1, 1982
Congenital generalized fibromatosis. Case report and literature review
P W Brill, D R Yandow, L O Langer, et al.
American Journal of Human Genetics
|
March 1, 1995
Genetic heterogeneity in multiple epiphyseal dysplasia
M Deere, S H Blanton, C I Scott, et al.
European Journal of Pediatrics
|
September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infants
E F Gilbert, J M Opitz, J W Spranger, et al.
Skeletal Radiology
|
January 1, 1991
Radiographic features of craniometadiaphyseal dysplasia, wormian bone type
L O Langer, P W Brill, E Afshani, et al.
Page
of 7