Prenatal exclusion of late infantile metachromatic leucodystrophy in a late-presenting pregnancy by assay of fetal leucocytes
- 1 July 1983
- journal article
- Published by Wiley in Prenatal Diagnosis
- Vol. 3 (3) , 257-259
- https://doi.org/10.1002/pd.1970030313
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Prenatal exclusion of homocystinuria (cystathionine β-synthase deficiency) by assay of phytohaemagglutinin-stimulated fetal lymphocytesPrenatal Diagnosis, 1983
- Prenatal exclusion of Hurler's disease by leucocyte α-L-iduronidase assayPrenatal Diagnosis, 1983
- A micromethod for the detection of arylsulfatases A and B in cultured fibroblasts and amniocytesAnalytical Biochemistry, 1982
- 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 a galactosaemia heterozygote by fetal blood enzyme assay.BMJ, 1979
- Sampling pure fetal blood by fetoscopy in second trimester of pregnancy.BMJ, 1978
- PRENATAL DIAGNOSIS OF MAROTEAUX-LAMY SYNDROMEThe Lancet, 1976
- Infantile Metachromatic LeukodystrophyNew England Journal of Medicine, 1973
- Metachromatic leukodystrophy:Clinical Genetics, 1973