PRENATAL DIAGNOSIS OF MAROTEAUX-LAMY SYNDROME
- 3 July 1976
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 308 (7975) , 50
- https://doi.org/10.1016/s0140-6736(76)93015-4
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Prenatal Diagnosis of Type II Glycogenosis (Pompe's Disease) Using Microchemical AnalysesPediatric Research, 1975
- Arylsulfatase B Deficiency in Maroteaux-Lamy Syndrome: Cellular Studies and Carrier IdentificationPediatric Research, 1975
- Dimethylaminoethanol for Tardive DyskinesiaNew England Journal of Medicine, 1975
- Arylsulfatase B deficiency in maroteaux-lamy syndrome cultured fibroblastsBiochemical and Biophysical Research Communications, 1974
- Methodology of the quantitative cytochemical analysis of single or small numbers of cultured cellsJournal of Molecular Histology, 1974
- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)American Journal of Diseases of Children, 1973
- A distinct biochemical deficit in the maroteaux-lamy syndrome (mucopolysaccharidosis VI)The Journal of Pediatrics, 1972
- THE DEFECT IN HURLER AND HUNTER SYNDROMES, II. DEFICIENCY OF SPECIFIC FACTORS INVOLVED IN MUCOPOLYSACCHARIDE DEGRADATIONProceedings of the National Academy of Sciences, 1969
- The assay of arylsulphatases A and B in human urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1959