IN-UTERO DETECTION OF TYPE-II GLYCOGENOSIS (POMPE'S DISEASE)
- 13 December 1969
- journal article
- Published by Elsevier in The Lancet
- Vol. 294 (7633) , 1277-1278
- https://doi.org/10.1016/s0140-6736(69)90811-3
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- CULTIVATED AMNIOTIC-FLUID CELLS AND FIBROBLASTS DERIVED FROM FAMILIES WITH CYSTIC FIBROSISThe Lancet, 1969
- Lesch-Nyhan Mutation: Prenatal Detection with Amniotic Fluid CellsScience, 1969
- Intrauterine Diagnosis of the Hurler and Hunter SyndromesNew England Journal of Medicine, 1969
- Enzymes in noncultured amniotic fluid cellsAmerican Journal of Obstetrics and Gynecology, 1969
- ANTENATAL DETECTION OF HEREDITARY DISORDERSPediatrics, 1968
- BIOCHEMICAL DIAGNOSIS OF AN X-LINKED DISEASE IN UTEROThe Lancet, 1968
- Patterns of enzyme development utilizing cultivated human fetal cells derived from amniotic fluidBiochemical Genetics, 1968
- α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)Biochemical Journal, 1963