Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era

The genetic basis for combined pituitary hormone deficiency (CPHD) is complex, involving 30 genes in a variety of syndromic and nonsyndromic presentations. Molecular diagnosis of this disorder is valuable for predicting disease progression, avoiding unnecessary surgery, and family planning. We expec...

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Dades bibliogràfiques
Publicat a:Endocr Rev
Autors principals: Fang, Qing, George, Akima S., Brinkmeier, Michelle L., Mortensen, Amanda H., Gergics, Peter, Cheung, Leonard Y. M., Daly, Alexandre Z., Ajmal, Adnan, Pérez Millán, María Ines, Ozel, A. Bilge, Kitzman, Jacob O., Mills, Ryan E., Li, Jun Z., Camper, Sally A.
Format: Artigo
Idioma:Inglês
Publicat: Endocrine Society 2016
Matèries:
Reviews
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5155665/
https://ncbi.nlm.nih.gov/pubmed/27828722
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/er.2016-1101
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