| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/EJHG.2011.142 |
| P8608 | Fatcat ID | release_suodihnfmnd2riz5d5mtoyudri |
| P932 | PMC publication ID | 3234510 |
| P698 | PubMed publication ID | 21863057 |
| P5875 | ResearchGate publication ID | 51591662 |
| P50 | author | Barbara Jarząb | Q16531491 |
| Sylwia Szpak-Ulczok | Q114413577 | ||
| P2093 | author name string | Egbert Schulze | |
| Friedhelm Raue | |||
| Karin Frank-Raue | |||
| Susanne Rondot | |||
| P2860 | cites work | Early Malignant Progression of Hereditary Medullary Thyroid Cancer | Q30320549 |
| Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis | Q34080215 | ||
| Guidelines for diagnosis and therapy of MEN type 1 and type 2. | Q34104591 | ||
| Studying the genetics of Hirschsprung's disease: unraveling an oligogenic disorder | Q35992939 | ||
| Diagnosis of pheochromocytoma with special emphasis on MEN2 syndrome | Q36463100 | ||
| RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumors | Q36540061 | ||
| Normal perioperative serum calcitonin levels in patients with advanced medullary thyroid carcinoma: case report and review of the literature. | Q37225664 | ||
| Medullary thyroid carcinoma without marked elevation of calcitonin: a diagnostic and surveillance dilemma | Q37225688 | ||
| Medullary thyroid cancer: management guidelines of the American Thyroid Association | Q37495961 | ||
| Molecular genetics and phenomics of RET mutations: Impact on prognosis of MTC. | Q37677251 | ||
| Update multiple endocrine neoplasia type 2. | Q37678245 | ||
| Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes | Q43861000 | ||
| RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center | Q46982081 | ||
| Estimation of risk of inherited medullary thyroid carcinoma in apparent sporadic patients. | Q52067452 | ||
| Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. | Q54638028 | ||
| Primary hyperparathyroidism in multiple endocrine neoplasia type 2A | Q71831532 | ||
| P433 | issue | 1 | |
| P921 | main subject | multiple endocrine neoplasia | Q1553018 |
| P304 | page(s) | 64-68 | |
| P577 | publication date | 2011-08-24 | |
| P1433 | published in | European Journal of Human Genetics | Q2155433 |
| P1476 | title | Clinical utility gene card for: multiple endocrine neoplasia type 2. | |
| P478 | volume | 20 |
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