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Publikováno v:
European Surgery. 25:55-57
Background Multiple endocrine neoplasia type I (MEN I) is a familial condition inherited in autosomal dominant manner, characterized by primary hyperparathyroidism (multiple gland hyperplasia 95%), pancreatic islet cell tumours (65%) and pituitary ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64fa057474878264544d3ef2b2b76574
https://doi.org/10.1007/bf02602037
https://doi.org/10.1007/bf02602037
