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Journal of Medical Genetics|April 1, 1976
Leucocyte values of alpha-L-iduronidase activity in mucopolysaccharidosis IT E Kelly, H A TaylorSouthern Medical Journal|November 1, 1979
Partial trisomy 4q resulting from a familial 4/3 translocationT E Kelly, R H Haslam, G H ThomasThe Journal of Pediatrics|May 1, 1976
Mannosidosis: phenotype of a severely affected child and characterization of alpha-mannosidase activity in cultured fibroblasts from the patient and his parentsA S Aylsworth, H A Taylor, C M Stuart, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 22, 1975
Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblastsH A Taylor, G H Thomas, A Aylsworth, et al.The Johns Hopkins Medical Journal|October 1, 1975
Mucolipidosis III (pseudo-Hurler polydystrophy): Clinical and laboratory studies in a series of 12 patientsT E Kelly, G H Thomas, H A Taylor, et al.American Journal of Medical Genetics|November 1, 1984
Teratogenicity of anticonvulsant drugs. III: Radiographic hand analysis of children exposed in utero to diphenylhydantoinT E KellyClinical Orthopaedics and Related Research|January 1, 1976
The mucopolysaccharidoses and mucolipidosesT E KellyHuman Mutation|January 1, 1992
Molecular basis of hexosaminidase A deficiency and pseudodeficiency in the Berks County Pennsylvania DutchE H Mules, S Hayflick, C E Dowling, et al.American Journal of Medical Genetics|January 1, 1977
Isolated acid neuraminidase deficiency: a distinct lysosomal storage diseaseT E Kelly, G GraetzPageof 22