Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture
- 30 September 1971
- journal article
- case report
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 79 (3), 366-378
- https://doi.org/10.1016/s0022-3476(71)80143-9
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- I-Cell Disease (Cont.)New England Journal of Medicine, 1970
- Hurler's Syndrome: Deficiency of a Specific Beta Galactosidase IsoenzymeScience, 1969
- Hurler and Hunter Syndromes: Mutual Correction of the Defect in Cultured FibroblastsScience, 1968
- The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.Proceedings of the National Academy of Sciences of the United States of America, 1968
- Mutant Enzymatic and Cytological Phenotypes in Cultured Human FibroblastsScience, 1967
- HURLER'S SYNDROMEThe Journal of Experimental Medicine, 1966
- The remarkable cells cultured from a human with Hurler’s syndrome: An approach to visual selection forin vitro genetic studiesIn Vitro Cellular & Developmental Biology - Plant, 1966
- HURLER'S SYNDROMEThe Journal of Experimental Medicine, 1966
- ELECTRON MICROSCOPY OF TWO CEREBRAL, BIOPSIES IN GARGOYLISMJournal of Neuropathology and Experimental Neurology, 1965
- HISTOCHEMICAL STUDIES IN HURLER'S DISEASE: A NEW METHOD FOR LOCALIZATION OF ACID MUCOPOLYSACCHARIDE, AND AN ANALYSIS OF LEAD ACETATE "FIXATION"Journal of Histochemistry & Cytochemistry, 1961