about
Co-occurrence of Sturge-Weber syndrome and Klippel-Trenaunay-Weber syndrome phenotype: Consideration of the historical aspect.Haploinsufficiency of NCOR1 associated with autism spectrum disorder, scoliosis, and abnormal palatogenesisCNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome
P50
description
researcher
@en
name
Yuri Sakaguchi
@en
type
label
Yuri Sakaguchi
@en
prefLabel
Yuri Sakaguchi
@en
P31
P496
0000-0002-5818-1110