A method for the prenatal diagnosis of congenital hyperuricemia
- 30 September 1969
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 75 (3) , 488-491
- https://doi.org/10.1016/s0022-3476(69)80279-9
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Prenatal detection of genetic defectsThe Journal of Pediatrics, 1969
- BIOCHEMICAL DIAGNOSIS OF AN X-LINKED DISEASE IN UTEROThe Lancet, 1968
- Chromatographic separation of nucleoside phosphates on diethylaminoethylcellulose paperAnalytical Biochemistry, 1968
- Patterns of enzyme development utilizing cultivated human fetal cells derived from amniotic fluidBiochemical Genetics, 1968
- The antepartum diagnosis of genetic diseasesThe Journal of Pediatrics, 1968
- Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine SynthesisScience, 1967
- A familial disorder of uric acid metabolism and central nervous system functionThe American Journal of Medicine, 1964
- Cyclic Phosphates. II. Further Studies of Ribonucleoside 2':3'-Cyclic Phosphates1Journal of the American Chemical Society, 1955