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Article

RET oligonucleotide microarray for the detection of RET mutations in multiple endocrine neoplasia type 2 syndromes.

Clinical cancer research : an official journal of the American Association for Cancer Research - 1 Feb 2002

Kim Il-Jin, Kang Hio Chung, Park Jae-Hyun, Ku Ja-Lok, Lee Jong-Soo, Kwon Hyuk-Joon, Yoon Kyong-Ah, Heo Seung Chul, Yang Hee-Young, Cho Bo Youn, Kim Seong Yeon, Oh Seung Keun, Youn Yeo-Kyu, Park Do-Jun, Lee Myung-Shik, Lee Kwang-Woo, Park Jae-Gahb

Abstract excerpt

Multiple endocrine neoplasia type 2 (MEN2) syndromes are inherited in an autosomal dominant fashion with high penetrance. There are three subtypes, namely, MEN2A (multiple endocrine neoplasia type 2A), MEN2B (multiple endocrine neoplasia type 2B), and familial medullary thyroid carcinoma. The variations in the RET gene play an important role in the MEN2 syndromes. In this work, we have developed a RET...

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PMID: 11839664

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RET

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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