Severe craniosynostosis with Noonan syndrome phenotype associated with SHOC2 mutation: Clinical evidence of crosslink between FGFR and RAS signaling pathways

Toshiki Takenouchi, Yoshiaki Sakamoto, Tomoru Miwa, Chiharu Torii, Rika Kosaki, Kazuo Kishi, Takao Takahashi, Kenjiro Kosaki

Research output: Contribution to journal › Article › peer-review

23 Citations (Scopus)

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Medicine & Life Sciences