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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1981
[Phenotypes in heteroglycanoses and sphingolipidoses (author's transl)]J GehlerHuman Genetics|June 29, 1976
The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolismM Cantz, J GehlerAmerican Journal of Medical Genetics|January 1, 1977
Mucolipidosis I--a sialidosisJ Sphranger, J Gehler, M CantzAmerican Journal of Medical Genetics|March 1, 1985
The clinical spectrum of alpha-L-iduronidase deficiencyM Roubicek, J Gehler, J SprangerKlinische Wochenschrift|June 1, 1979
Comprehensive urinary screening for inborn errors of complex carbohydrate metabolismA C Sewell, J Gehler, J SprangerEuropean Journal of Pediatrics|May 1, 1980
Urinary oligosaccharide screening in patients with beta-galactosidase deficiencyA C Sewell, J Gehler, J SprangerEuropean Journal of Pediatrics|June 8, 1976
Prenatal diagnosis of mucolipidosis II (I-cell disease)J Gehler, M Cantz, M Stoeckenius, et al.Journal of Medical Genetics|April 1, 1978
Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromesB Zabel, W Baumann, J Gehler, et al.Geburtshilfe Und Frauenheilkunde|November 1, 1988
[Prenatal diagnosis of sialidosis, a defect of the lysosomal enzyme neuraminidase]H Heyes, J Gehler, U Töllner, et al.Pageof 3