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Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity.
- Published in:
- Frontiers in Endocrinology, 2020, v. 11, p. 1, doi. 10.3389/fendo.2020.00081
- By:
- Publication type:
- Article
Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort.
- Published in:
- Thyroid, 2016, v. 26, n. 9, p. 1215, doi. 10.1089/thy.2016.0016
- By:
- Publication type:
- Article
Pediatric Cushing's disease due to pituitary hyperplasia.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
A pragmatic controlled trial to prevent childhood obesity within a risk group at maternity and child health-care clinics: results up to six years of age (the VACOPP study).
- Published in:
- 2018
- By:
- Publication type:
- journal article
Pragmatic controlled trial to prevent childhood obesity in maternity and child health care clinics: pregnancy and infant weight outcomes (The VACOPP Study).
- Published in:
- BMC Pediatrics, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2431-13-80
- By:
- Publication type:
- Article
Pragmatic controlled trial to prevent childhood obesity in maternity and child health care clinics: pregnancy and infant weight outcomes (the VACOPP Study).
- Published in:
- 2013
- By:
- Publication type:
- journal article
Behavioral counseling to prevent childhood obesity--study protocol of a pragmatic trial in maternity and child health care.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Behavioral counseling to prevent childhood obesity -- study protocol of a pragmatic trial in maternity and child health care.
- Published in:
- BMC Pediatrics, 2012, v. 12, n. 1, p. 93, doi. 10.1186/1471-2431-12-93
- By:
- Publication type:
- Article
Targeted Exome Sequencing of Genes Involved in Rare CNVs in Early-Onset Severe Obesity.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.839349
- By:
- Publication type:
- Article