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Deutsche Medizinische Wochenschrift (1946)|December 14, 1979
[Treatment of osteogenesis imperfecta with (+)-catechin (author's transl)]H Stöss, H J Pesch, J Spranger
American Journal of Medical Genetics|December 8, 1998
Progressive laryngotracheal stenosis with short stature and arthropathyR J Hopkin, R Cotton, L O Langer, et al.
American Journal of Medical Genetics|October 1, 1983
Brachyolmia, recessive type (Hobaek): a clinical, radiographic, and histochemical studyW A Horton, L O Langer, D L Collins, et al.
Clinical Genetics|April 1, 1986
Heterogeneity of Morquio diseaseM Beck, J Glössl, A Grubisic, et al.
European Journal of Pediatrics|August 13, 1999
Abnormal subcortical somatosensory evoked potentials indicate high cervical myelopathy in achondroplasiaR Boor, G Fricke, K Brühl, et al.
Klinische Padiatrie|July 1, 1976
[Vater or Vacterl syndrome (author's transl)]W Baumann, I Greinacher, P Emmrich, et al.
American Journal of Medical Genetics|October 1, 1993
Cognitive skills in achondroplasiaG Brinkmann, H Schlitt, P Zorowka, et al.
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
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