Rapid Mutation Screening for HRPT2 and MEN1 Mutations Associated with Familial and Sporadic Primary Hyperparathyroidism

Familial hyperparathyroidism, a disease of the parathyroid glands, may occur in conjunction with pituitary and pancreatic tumors (multiple endocrine neoplasia type I), kidney and bone tumors (hyperparathyroidism jaw tumor syndrome), or alone (familial isolated hyperparathyroidism). This study descri...

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Detalhes bibliográficos
Main Authors: Howell, Viive M., Cardinal, John W., Richardson, Anne-Louise, Gimm, Oliver, Robinson, Bruce G., Marsh, Deborah J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2006
Assuntos:
Regular Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1876168/
https://ncbi.nlm.nih.gov/pubmed/17065424
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2006.060015
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