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American Journal of Medical Genetics|March 1, 1985
The clinical spectrum of alpha-L-iduronidase deficiencyM Roubicek, J Gehler, J SprangerEuropean Journal of Pediatrics|February 1, 1994
The type II collagenopathies: a spectrum of chondrodysplasiasJ Spranger, A Winterpacht, B ZabelAmerican Journal of Medical Genetics|March 3, 1997
Kniest dysplasia: Dr. W. Kniest, his patient, the molecular defectJ Spranger, A Winterpacht, B ZabelAmerican Journal of Medical Genetics|October 1, 1990
Chondrodysplasia punctata, tibia-metacarpal (MT) typeM Rittler, H Menger, J SprangerPediatric Radiology|January 1, 1982
Osteogenesis imperfecta congenita. Features and prognosis of a heterogenous conditionJ Spranger, B Cremin, P BeightonMechanisms of Development|March 12, 1999
Regulation of chondrocyte differentiation by Cbfa1I S Kim, F Otto, B Zabel, et al.Science (New York, N.Y.)|April 26, 1996
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13Y Muragaki, S Mundlos, J Upton, et al.Bone|January 1, 1990
Distribution of type I and type II collagen gene expression during the development of human long bonesS Mundlos, H Engel, I Michel-Behnke, et al.American Journal of Medical Genetics|May 3, 1996
An alpha 1(II) Gly913 to Cys substitution prevents the matrix incorporation of type II collagen which is replaced with type I and III collagens in cartilage from a patient with hypochondrogenesisS Mundlos, D Chan, J McGill, et al.Pageof 23