Found: 3
Select item for more details and to access through your institution.
Divergent Metabolic Phenotype between Two Sisters with Congenital Generalized Lipodystrophy Due to Double AGPAT2 Homozygous Mutations. A Clinical, Genetic and <i>In Silico</i> Study.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0087173
- By:
- Publication type:
- Article
Association between eating behavior scores and obesity in Chilean children.
- Published in:
- 2011
- By:
- Publication type:
- journal article
APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.
- Published in:
- BMC Medical Genetics, 2012, v. 13, n. 1, p. 106, doi. 10.1186/1471-2350-13-106
- By:
- Publication type:
- Article