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European Journal of Pediatrics|March 1, 1983
Progressive pseudorheumatoid arthritis of childhood (PPAC). A hereditary disorder simulating rheumatoid arthritisJ Spranger, C Albert, F Schilling, et al.European Journal of Pediatrics|August 17, 1978
Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrumJ Spranger, M Cantz, J Gehler, et al.Clinical Dysmorphology|January 11, 2001
Ischiospinal dysostosis with rib gaps and nephroblastomatosisJ Spranger, S Self, K B Clarkson, et al.American Journal of Medical Genetics. Part A|August 19, 2003
Congenital generalized lipodystrophy, mental retardation, deafness, short stature, and slender bones: a newly recognized syndrome?A Rajab, M Khaburi, S Spranger, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 1, 1997
Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant miceL F Huang, N Fukai, P B Selby, et al.Klinische Padiatrie|November 1, 1975
[Congenital spondylo-epiphyseal dysplasia: follow-up of a case over 9 years (author's transl)]T Luthardt, H Reinwein, H Schönenberg, et al.Archives of Gynecology and Obstetrics|August 29, 2002
Malformations in newborn: results based on 30,940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998)A Queisser-Luft, G Stolz, A Wiesel, et al.European Journal of Pediatrics|June 1, 1983
Heterogeneity of metatropic dysplasiaM Beck, M Roubicek, J G Rogers, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristicsJ Gehler, A C Sewell, C Becker, et al.Helvetica Paediatrica Acta|January 1, 1981
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian familyJ Gehler, A C Sewell, C Becker, et al.Pageof 23