scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0002-9343(80)80013-1 |
P698 | PubMed publication ID | 6108714 |
P2093 | author name string | S Buehler | |
N R Farid | |||
N A Russell | |||
H S Smyth | |||
F B Maroun | |||
P Allerdice | |||
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Prolactin and thyrotropin release in man by synthetic pyroglutamyl-histidyl-prolinamide | Q67234928 | ||
Carcinoid of the thymus with hereditary hyperparathyroidism | Q67374636 | ||
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P433 | issue | 6 | |
P921 | main subject | multiple endocrine neoplasia | Q1553018 |
carcinoid tumor | Q1734755 | ||
P304 | page(s) | 874-880 | |
P577 | publication date | 1980-12-01 | |
P1433 | published in | American Journal of Medicine | Q2842959 |
P1476 | title | Prolactinomas in familial multiple endocrine neoplasia syndrome type I. Relationship to HLA and carcinoid tumors | |
P478 | volume | 69 |
Q60021682 | 10 Multiple endocrine neoplasia |
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Q71827858 | Genetic screening to identify the gene carrier in Italian and German kindreds affected by multiple endocrine neoplasia type 1 (MEN 1) syndrome |
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Q35889219 | Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland |
Q62978448 | Multiple endocrine neoplasia syndromes |
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Q40471503 | Multiple endocrine neoplasia type 1 (MEN 1) revisited |
Q28214101 | Multiple endocrine neoplasia type 1Burin from Mauritius: a novel MEN1 mutation |
Q36496864 | Multiple endocrine neoplasia type I: general features and new insights into etiology |
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Q28210134 | The MEN1 gene and associated diseases: an update |
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Q40624170 | The role of molecular genetics in screening for multiple endocrine neoplasia type 1. |
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Q73015245 | [Multiple endocrine neoplasia Type I. Diagnosis and therapy in a case with classical family history] |
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