Author:
Clayton P. T.,Eckhardt S.,Wilson J.,Hall C. M.,Yousuf Y.,Wanders R. J. A.,Schutgens R. B. H.
Subject
Genetics (clinical),Genetics
Reference18 articles.
1. Barr DGD, Kirk JM, Al Howasi M, Wanders RJA, Schutgens RBH (1993) Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.Arch Dis Child 68: 415?417.
2. Björkhem I, Sisfontes L, Boström B, Kase BF, Blomstrand R (1986) Simple diagnosis of the Zellweger syndrome by gas liquid chromatography of dimethylacetals.J Lipid Res 27: 786?791.
3. Clayton PT, Thompson M (1988) Dysmorphic syndromes with demonstrable biochemical abnormalities.J Med Genet 25: 463?472.
4. Clayton PT, Kalter C, Atheron DJ, Besley GTN, Broadhead DM (1989) Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndrome.J Inher Metab Dis 12 (supplement 2): 358?360.
5. Heikoop JC, Wanders RJ, Strijland A, Purvis R, Schutgens RBH, Tager JM (1992) Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata.Hum Genet 89: 439?444.
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