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August 22, 1996International Journal of CancerOpen Access

Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of theRET proto-oncogene

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Authors

MFMonika FinkUniversität InnsbruckAWAndreas WeinhäuselAustrian Institute of TechnologyBNBruno NiederleMedical University of Vienna

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Fink et al. (1996) studied this question.

synapsesocial.com/papers/6aa1273d372f0d69599d2d7fhttps://doi.org/10.1002/(sici)1097-0215(19960822)69:4<312::aid-ijc13>3.0.co;2-7
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Somatic mutations in the <i>RET</i> proto‐oncogene in sporadic medullary thyroid carcinoma1996 · 278 citations
  2. 2Clinical Screening as Compared with DNA Analysis in Families with Multiple Endocrine Neoplasia Type 2A1994 · 456 citations
  3. 3Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC1993 · 1,310 citations
  4. 4Single missense mutation in the tyrosine kinasecatalytic domain of the RET protooncogene is associated with multiple endocrineneoplasia type 2B.1994 · 602 citations
  5. 5Mutation of the <i>RET</i> protooncogene in sporadic medullary thyroid carcinoma1995 · 160 citations