Iduronate sulfatase in amniotic fluid: An aid in the prenatal diagnosis of the Hunter syndrome
- 31 March 1977
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 90 (3), 423-425
- https://doi.org/10.1016/s0022-3476(77)80707-5
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Present status of intrauterine diagnosis of genetic defectsAmerican Journal of Obstetrics and Gynecology, 1974
- Demonstration of the Heterozygous State in Hunter's SyndromePediatrics, 1974
- Hunter's syndrome: A deficiency of L-idurono-sulfate sulfataseBiochemical and Biophysical Research Communications, 1973
- The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate SulfataseProceedings of the National Academy of Sciences, 1973
- Intrauterine Diagnosis of the Hurler and Hunter SyndromesNew England Journal of Medicine, 1969