Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1984 Oct;21(5):397. doi: 10.1136/jmg.21.5.397

A case of 2-methylacetoacetyl CoA thiolase deficiency with coincidental chromosome abnormalities.

R G Gray, G W Lowther, J M Littlewood, B Middleton, M J Bennett
PMCID: PMC1049330  PMID: 6150117

Full text

PDF

Page 397

397

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Schutgens R. B., Middleton B., vd Blij J. F., Oorthuys J. W., Veder H. A., Vulsma T., Tegelaers W. H. Beta-ketothiolase deficiency in a family confirmed by in vitro enzymatic assays in fibroblasts. Eur J Pediatr. 1982 Sep;139(1):39–42. doi: 10.1007/BF00442077. [DOI] [PubMed] [Google Scholar]
  2. Tiepolo L., Zuffardi O., Fraccaro M., di Natale D., Gargantini L., Müller C. R., Ropers H. H. Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. Hum Genet. 1980;54(2):205–206. doi: 10.1007/BF00278973. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES