ANTENATAL DIAGNOSIS OF COMBINED XANTHINE AND SULPHITE OXIDASE DEFICIENCIES
- 1 December 1983
- journal article
- Published by Elsevier in The Lancet
- Vol. 322 (8363) , 1363-1364
- https://doi.org/10.1016/s0140-6736(83)91118-2
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROMEThe Lancet, 2003
- Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenaseJournal of Inherited Metabolic Disease, 1983
- Ultrasound imaging in the diagnosis of muscle diseaseThe Journal of Pediatrics, 1982
- Deletions of Chromosome 15 as a Cause of the Prader–Willi SyndromeNew England Journal of Medicine, 1981
- Needle muscle biopsy for carrier detection in Duchenne muscular dystrophyJournal of the Neurological Sciences, 1981
- Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.Proceedings of the National Academy of Sciences, 1980