Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Spranger

Showing results (111-120 of 247) with videos related to

Pageof 25
Sort By:
American Journal of Medical Genetics|September 1, 1987
Further delineation of the 3-M syndrome with review of the literatureR C Hennekam, J B Bijlsma, J Spranger
American Journal of Medical Genetics|March 1, 1989
Micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification: another observationP Meinecke, J Spranger, E Schaefer, et al.
European Journal of Pediatrics|June 8, 1976
Prenatal diagnosis of mucolipidosis II (I-cell disease)J Gehler, M Cantz, M Stoeckenius, et al.
European Journal of Pediatrics|May 1, 1995
Environmental aspects in pediatrics. New item in the European Journal of PediatricsK E von Mühlendahl, M Otto, J Spranger
The Journal of Bone and Joint Surgery. American Volume|March 1, 1970
Pyle's disease (familial metaphyseal dysplasia). A presentation of two cases and argument for its separation from craniometaphyseal dysplasiaR J Gorlin, M F Koszalka, J Spranger
Scandinavian Journal of Gastroenterology|July 2, 1998
Increased serum levels of vascular endothelial growth factor in patients with inflammatory bowel diseaseT Griga, A Tromm, J Spranger, et al.
American Journal of Medical Genetics|June 24, 1998
A rare form of spondylometaphyseal dysplasia-type A4T Duetting, A Schulze, J Troeger, et al.
Virchows Archiv. B, Cell Pathology|January 1, 1971
Hepatic ultrastructure in chondroitin-4-sulfate mucopolysaccharidosisF Freitag, K Küchemann, W Schuster, et al.
Radiology|February 1, 1975
The Dyggve-Melchior-Clausen syndromeJ Spranger, P Maroteaux, V M Der Kaloustian
American Journal of Medical Genetics|February 1, 1983
Progressive pseudorheumatoid arthropathy of childhood (PPAC): a hereditary disorder simulating juvenile rheumatoid arthritisJ Spranger, C Albert, F Schilling, et al.
Pageof 25

Showing results (111-120 of 247) with videos related to

Sort By:
Pageof 25
American Journal of Medical Genetics|September 1, 1987
Further delineation of the 3-M syndrome with review of the literatureR C Hennekam, J B Bijlsma, J Spranger
American Journal of Medical Genetics|March 1, 1989
Micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification: another observationP Meinecke, J Spranger, E Schaefer, et al.
European Journal of Pediatrics|June 8, 1976
Prenatal diagnosis of mucolipidosis II (I-cell disease)J Gehler, M Cantz, M Stoeckenius, et al.
European Journal of Pediatrics|May 1, 1995
Environmental aspects in pediatrics. New item in the European Journal of PediatricsK E von Mühlendahl, M Otto, J Spranger
The Journal of Bone and Joint Surgery. American Volume|March 1, 1970
Pyle's disease (familial metaphyseal dysplasia). A presentation of two cases and argument for its separation from craniometaphyseal dysplasiaR J Gorlin, M F Koszalka, J Spranger
Scandinavian Journal of Gastroenterology|July 2, 1998
Increased serum levels of vascular endothelial growth factor in patients with inflammatory bowel diseaseT Griga, A Tromm, J Spranger, et al.
American Journal of Medical Genetics|June 24, 1998
A rare form of spondylometaphyseal dysplasia-type A4T Duetting, A Schulze, J Troeger, et al.
Virchows Archiv. B, Cell Pathology|January 1, 1971
Hepatic ultrastructure in chondroitin-4-sulfate mucopolysaccharidosisF Freitag, K Küchemann, W Schuster, et al.
Radiology|February 1, 1975
The Dyggve-Melchior-Clausen syndromeJ Spranger, P Maroteaux, V M Der Kaloustian
American Journal of Medical Genetics|February 1, 1983
Progressive pseudorheumatoid arthropathy of childhood (PPAC): a hereditary disorder simulating juvenile rheumatoid arthritisJ Spranger, C Albert, F Schilling, et al.
Pageof 25