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Verhandlungen Der Deutschen Gesellschaft Fur Pathologie
|
January 1, 1970
[Formation of storage elements in liver cells in lipomucopolysaccharidosis]
F Freitag, J Spranger, S Blümcke
European Journal of Pediatrics
|
February 1, 1994
The type II collagenopathies: a spectrum of chondrodysplasias
J Spranger, A Winterpacht, B Zabel
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie
|
January 1, 1971
[Comparative ultrastructural investigations of livers in mucopolysaccharidoses and mucolipidoses (author's transl)]
S Blümcke, F Freitag, J Spranger
American Journal of Medical Genetics
|
March 3, 1997
Kniest dysplasia: Dr. W. Kniest, his patient, the molecular defect
J Spranger, A Winterpacht, B Zabel
American Journal of Medical Genetics
|
October 1, 1990
Chondrodysplasia punctata, tibia-metacarpal (MT) type
M Rittler, H Menger, J Spranger
Pediatric Radiology
|
January 1, 1982
Osteogenesis imperfecta congenita. Features and prognosis of a heterogenous condition
J Spranger, B Cremin, P Beighton
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie
|
October 1, 1974
Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfatase
J F O'Brien, J Spranger, M Cantz
Progress in Clinical and Biological Research
|
January 1, 1982
Different morphologic findings and genetic heterogeneity in pseudoachondroplasia: light- and electron-microscopic observations in iliac crest bioptic material
H Stöss, H J Pesch, J Spranger
Klinische Wochenschrift
|
June 1, 1979
Comprehensive urinary screening for inborn errors of complex carbohydrate metabolism
A C Sewell, J Gehler, J Spranger
Annals of the New York Academy of Sciences
|
January 1, 1988
Heterogeneity in osteogenesis imperfecta: clinical and morphological findings
B F Pontz, H Stöss, J Spranger
Page
of 25
Search research articles
Search
Showing results (81-90 of 247) with videos related to
Sort By:
Page
of 25
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie
|
January 1, 1970
[Formation of storage elements in liver cells in lipomucopolysaccharidosis]
F Freitag, J Spranger, S Blümcke
European Journal of Pediatrics
|
February 1, 1994
The type II collagenopathies: a spectrum of chondrodysplasias
J Spranger, A Winterpacht, B Zabel
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie
|
January 1, 1971
[Comparative ultrastructural investigations of livers in mucopolysaccharidoses and mucolipidoses (author's transl)]
S Blümcke, F Freitag, J Spranger
American Journal of Medical Genetics
|
March 3, 1997
Kniest dysplasia: Dr. W. Kniest, his patient, the molecular defect
J Spranger, A Winterpacht, B Zabel
American Journal of Medical Genetics
|
October 1, 1990
Chondrodysplasia punctata, tibia-metacarpal (MT) type
M Rittler, H Menger, J Spranger
Pediatric Radiology
|
January 1, 1982
Osteogenesis imperfecta congenita. Features and prognosis of a heterogenous condition
J Spranger, B Cremin, P Beighton
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie
|
October 1, 1974
Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfatase
J F O'Brien, J Spranger, M Cantz
Progress in Clinical and Biological Research
|
January 1, 1982
Different morphologic findings and genetic heterogeneity in pseudoachondroplasia: light- and electron-microscopic observations in iliac crest bioptic material
H Stöss, H J Pesch, J Spranger
Klinische Wochenschrift
|
June 1, 1979
Comprehensive urinary screening for inborn errors of complex carbohydrate metabolism
A C Sewell, J Gehler, J Spranger
Annals of the New York Academy of Sciences
|
January 1, 1988
Heterogeneity in osteogenesis imperfecta: clinical and morphological findings
B F Pontz, H Stöss, J Spranger
Page
of 25