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STUDY OF A KINDRED WITH PHEOCHROMOCYTOMA, MEDULLARY THYROID CARCINOMA, HYPERPARATHYROIDISM AND GUSHING ʼS DISEASE: MULTIPLE ENDOCRINE NEOPLASIA, TYPE 21
Medicine · 1968 · Vol. 47(5) · pp. 371–409
Alton L. Steiner✉(United States Public Health Service)Andrew Goodman(United States Public Health Service)Samuel Ralph Powers(Albany Medical Center Hospital)
Abstract
2This research was supported by U. S. Public Health Service research grants 5-MO1-FR00094 CLR from the Division of Research Facilities and Resources, and GRS-FR 5394 3Work done during the term of U. S. Public Health Service Postdoctoral Fellowship 5-F2-AM- 28,805. Current address: Metabolism Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 4From the Subdepartment of Endocrinology and Metabolism, Department of Medicine, and the Department of Surgery, Albany Medical College, and the Albany Medical Center Hospital, Albany, New York
Neuroendocrine Tumor Research AdvancesMetabolism, Diabetes, and CancerPituitary Gland Disorders and TreatmentsMedicinePublic healthHyperparathyroidismThyroid carcinomaThyroidEndocrine diseasePheochromocytomaMultiple endocrine neoplasiaFamily medicineEndocrine system
MeSH terms
AdolescentAdultAgedChildChild, PreschoolCushing SyndromeFemaleHumansMaleMiddle AgedMultiple Endocrine NeoplasiaParathyroid NeoplasmsPedigreePheochromocytomaThyroid Neoplasms
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