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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.
Behavioral Neuroscience|September 11, 1998
Comparison of the amnestic effects of NMDA receptor antagonist MK-801 and nitric oxide synthase inhibitors: L-NAME and L-NOARG in goldfishX Xu, W Boshoven, B Lombardo, 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.
Pediatric Radiology|January 1, 1988
Metaphyseal chondrodysplasia, Schmid type. Clinical and radiographic delineation with a review of the literatureR S Lachman, D L Rimoin, J Spranger
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
European Journal of Pediatrics|June 8, 1976
Prenatal diagnosis of mucolipidosis II (I-cell disease)J Gehler, M Cantz, M Stoeckenius, et al.
Nature|March 28, 1991
Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporterE Turk, B Zabel, S Mundlos, et al.
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.
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