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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Endocrine Society 2012
Pynciau:
JCEM Online: Advances in Genetics
Mynediad Ar-lein: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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