PRENATAL DIAGNOSIS OF NIEMANN-PICK DISEASE TYPE A USING CHROMOGENIC SUBSTRATE
- 16 July 1977
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 310 (8029) , 144
- https://doi.org/10.1016/s0140-6736(77)90159-3
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- A Practical Chromogenic Procedure for the Detection of Homozygotes and Heterozygous Carriers of Niemann-Pick DiseaseNew England Journal of Medicine, 1975
- Identification of heterozygous carriers of lipid storage diseasesThe American Journal of Medicine, 1971
- Deficiency of sphingomyelin-cleaving enzyme activity in tissue cultures derived from patients with Niemann-Pick diseaseBiochemical and Biophysical Research Communications, 1969
- Diagnosis of Gaucher's Disease and Niemann-Pick Disease with Small Samples of Venous BloodScience, 1967
- Enzymatic Hydrolysis of SphingolipidsPublished by Elsevier ,1966