Zellweger syndrome and a microdeletion of the proximal long arm of chromosome 7
- 1 October 1988
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 80 (2) , 201-202
- https://doi.org/10.1007/bf00702873
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Peroxisomal disorders: A newly recognised group of genetic diseasesEuropean Journal of Pediatrics, 1986
- Peroxisomal disordersThe Journal of Pediatrics, 1986
- The Peroxisomal DisordersHospital Practice, 1985
- Peroxisomal β-oxidation enzyme proteins in the Zellweger syndromeBiochemical and Biophysical Research Communications, 1985
- Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndromeBiochemical and Biophysical Research Communications, 1984
- Interstitial deletion of a chromosome 7 (q11.2q22.1) in a child with splithand/splitfoot malformation.1984
- Interstitial deletion of chromosome 7: A case report and review of the literatureClinical Genetics, 1982