Yuri Sakaguchi
4PUBLICATIONS
2CO-AUTHORS
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Publications (4)
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|Dec 28, 2020
Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis.Yuri Sakaguchi, Hiroshi Yoshihashi, Tomoko Uehara
|Feb 16, 2019
CNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome.Tomoko Uehara, Toshiki Takenouchi, Yu Yamaguchi
|Oct 06, 2018
Haploinsufficiency of NCOR1 associated with autism spectrum disorder, scoliosis, and abnormal palatogenesis.Yuri Sakaguchi, Tomoko Uehara, Hisato Suzuki
|Aug 08, 2017
Co-occurrence of Sturge-Weber syndrome and Klippel-Trenaunay-Weber syndrome phenotype: Consideration of the historical aspect.Yuri Sakaguchi, Toshiki Takenouchi, Tomoko Uehara
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