The MENX Syndrome and p27: Relationships with Multiple Endocrine Neoplasia
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Elsevier
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1. Germline CDKN1B variant type and site are associated with phenotype in MEN4;Endocrine-Related Cancer;2023-01-01
2. Hereditary Parathyroid Disease: Sometimes Pathologists Do Not Know What They Are Missing;Endocrine Pathology;2020-05-28
3. Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing’s Disease With or Without an MEN4 Phenotype;The Journal of Clinical Endocrinology & Metabolism;2020-03-31
4. Diagnosis of mosaic mutations in the MEN1 gene by next generation sequencing;European Journal of Endocrinology;2019-02
5. Molekuláris genetikai vizsgálatok az örökletes endokrinológiai tumor szindrómák klinikai diagnosztikájában;Orvosi Hetilap;2018-02
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