FLUORIMETRIC ASSAY FOR PRENATAL DETECTION OF HURLER AND SCHEIE HOMOZYGOTES OR HETEROZYGOTES
- 21 January 1978
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 311 (8056), 147
- https://doi.org/10.1016/s0140-6736(78)90441-5
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Fibroblast phosphodiesterase deficiency in Niemann-Pick diseaseBiochemical and Biophysical Research Communications, 1977
- Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1975
- A method for α‐L‐iduronidase assayFEBS Letters, 1974
- α-l-Iduronidase activity in cultured skin fibroblasts and amniotic fluid cellsArchives of Biochemistry and Biophysics, 1973
- Genetic Errors of Mucopolysaccharide DegradationBiochemical Society Transactions, 1973
- I-Cell Disease: Biochemical StudiesPediatric Research, 1972
- The Defect in the Hurler and Scheie Syndromes: Deficiency of α-L-IduronidaseProceedings of the National Academy of Sciences, 1972
- Hurler's syndrome, an a-L-iduronidase deficiencyBiochemical and Biophysical Research Communications, 1972
- ALLELISM, NON-ALLELISM, AND GENETIC COMPOUNDS AMONG THE MUCOPOLYSACCHARIDOSESThe Lancet, 1972
- Tay-Sachs Disease: Prenatal DiagnosisScience, 1971