Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.
Publication
, Journal Article
Irizarry, KA; Miller, M; Freemark, M; Haqq, AM
Published in: Adv Pediatr
August 2016
Duke Scholars
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Published In
Adv Pediatr
DOI
EISSN
1878-1926
Publication Date
August 2016
Volume
63
Issue
1
Start / End Page
47 / 77
Location
United States
Related Subject Headings
- Sleep Wake Disorders
- Prader-Willi Syndrome
- Pediatrics
- Obesity
- Mental Disorders
- Hypothyroidism
- Hypogonadism
- Hyperphagia
- Humans
- Human Growth Hormone
Citation
APA
Chicago
ICMJE
MLA
NLM
Irizarry, K. A., Miller, M., Freemark, M., & Haqq, A. M. (2016). Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy. Adv Pediatr, 63(1), 47–77. https://doi.org/10.1016/j.yapd.2016.04.005
Irizarry, Krystal A., Mark Miller, Michael Freemark, and Andrea M. Haqq. “Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.” Adv Pediatr 63, no. 1 (August 2016): 47–77. https://doi.org/10.1016/j.yapd.2016.04.005.
Irizarry KA, Miller M, Freemark M, Haqq AM. Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy. Adv Pediatr. 2016 Aug;63(1):47–77.
Irizarry, Krystal A., et al. “Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.” Adv Pediatr, vol. 63, no. 1, Aug. 2016, pp. 47–77. Pubmed, doi:10.1016/j.yapd.2016.04.005.
Irizarry KA, Miller M, Freemark M, Haqq AM. Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy. Adv Pediatr. 2016 Aug;63(1):47–77.
Published In
Adv Pediatr
DOI
EISSN
1878-1926
Publication Date
August 2016
Volume
63
Issue
1
Start / End Page
47 / 77
Location
United States
Related Subject Headings
- Sleep Wake Disorders
- Prader-Willi Syndrome
- Pediatrics
- Obesity
- Mental Disorders
- Hypothyroidism
- Hypogonadism
- Hyperphagia
- Humans
- Human Growth Hormone