Search filters

List of works by Yuri Sakaguchi

CNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome

scientific article published on 15 February 2019

Co-occurrence of Sturge-Weber syndrome and Klippel-Trenaunay-Weber syndrome phenotype: Consideration of the historical aspect.

scientific article

Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis

scientific article published on 27 December 2020

Haploinsufficiency of NCOR1 associated with autism spectrum disorder, scoliosis, and abnormal palatogenesis

scientific article published on 05 October 2018

Paulina is supported by:

About Paulina

Help