Prenatal exclusion of Hurler's disease by leucocyte α-L-iduronidase assay
- 1 January 1983
- journal article
- case report
- Published by Wiley in Prenatal Diagnosis
- Vol. 3 (1) , 61-63
- https://doi.org/10.1002/pd.1970030113
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Correct prenatal diagnosis of a hurler fetus where amniotic fluid cell cultures were of maternal originPrenatal Diagnosis, 1981
- FETOSCOPY GUIDED BY REAL‐TIME ULTRASOUND FOR PURE FETAL BLOOD SAMPLES, FETAL SKIN SAMPLES, AND EXAMINATION OF THE FETUS IN UTEROBJOG: An International Journal of Obstetrics and Gynaecology, 1980
- PRENATAL DIAGNOSIS OF FARBER'S DISEASEThe Lancet, 1979
- PRENATAL DIAGNOSIS OF TWO HURLER FETUSES USING AN IMPROVED ASSAY FOR METHYLUMBELLIFERYL-α-L-IDURONEDASEThe Lancet, 1979
- Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assay.BMJ, 1979
- Sampling pure fetal blood by fetoscopy in second trimester of pregnancy.BMJ, 1978
- A method for the determination of amniotic-fluid glycosaminoglycans and its application to the prenatal diagnosis of hurler and sanfilippo diseasesClinica Chimica Acta; International Journal of Clinical Chemistry, 1977