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Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.
Irizarry, Krystal A; Miller, Mark; Freemark, Michael; Haqq, Andrea M.
  • Irizarry KA; Division of Pediatric Endocrinology, Duke University Medical Center, 3000 Erwin Road, Suite 200, Durham, NC 27705, USA.
  • Miller M; Division of Pediatric Endocrinology, Duke University Medical Center, 3000 Erwin Road, Suite 200, Durham, NC 27705, USA.
  • Freemark M; Division of Pediatric Endocrinology, Duke University Medical Center, 3000 Erwin Road, Suite 200, Durham, NC 27705, USA.
  • Haqq AM; Division of Pediatric Endocrinology, University of Alberta, 1C4 Walter C. Mackenzie Health Sciences Center, 8440 - 112 Street Northwest, Edmonton, Alberta T6G 2R7, Canada. Electronic address: haqq@ualberta.ca.
Adv Pediatr ; 63(1): 47-77, 2016 08.
Article en En | MEDLINE | ID: mdl-27426895
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Child / Humans Idioma: En Año: 2016 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Child / Humans Idioma: En Año: 2016 Tipo del documento: Article