Severe craniosynostosis with Noonan syndrome phenotype...

American Journal of Medical Genetics Part A 2014 / 11 Vol. 164; Iss. 11

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

Takenouchi, Toshiki, Sakamoto, Yoshiaki, Miwa, Tomoru, Torii, Chiharu, Kosaki, Rika, Kishi, Kazuo, Takahashi, Takao, Kosaki, Kenjiro
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Volume:
164
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.36705
Date:
November, 2014
File:
PDF, 348 KB
english, 2014
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