Genetic Overlap in Kallmann Syndrome, Combined Pituitary Hormone Deficiency, and Septo-Optic Dysplasia

CONTEXT: Kallmann syndrome (KS), combined pituitary hormone deficiency (CPHD), and septo-optic dysplasia (SOD) all result from development defects of the anterior midline in the human forebrain. OBJECTIVE: The objective of the study was to investigate whether KS, CPHD, and SOD have shared genetic or...

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Bibliografische gegevens
Hoofdauteurs: Raivio, Taneli, Avbelj, Magdalena, McCabe, Mark J., Romero, Christopher J., Dwyer, Andrew A., Tommiska, Johanna, Sykiotis, Gerasimos P., Gregory, Louise C., Diaczok, Daniel, Tziaferi, Vaitsa, Elting, Mariet W., Padidela, Raja, Plummer, Lacey, Martin, Cecilia, Feng, Bihua, Zhang, Chengkang, Zhou, Qun-Yong, Chen, Huaibin, Mohammadi, Moosa, Quinton, Richard, Sidis, Yisrael, Radovick, Sally, Dattani, Mehul T., Pitteloud, Nelly
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Endocrine Society 2012
Onderwerpen:
JCEM Online: Advances in Genetics
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3319178/
https://ncbi.nlm.nih.gov/pubmed/22319038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2011-2938
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