<i>SMARCE1</i>, a rare cause of Coffin–Siris Syndrome: Clinical description of three additional cases
Yuri A. Zárate(University of Kentucky), Samantha A. Schrier Vergano(Children's Hospital of The King's Daughters), Yoshinori Tsurusaki(Yokohama City University), Luis Escobar(St. Vincent Hospital), Naomichi Matsumoto(Yokohama City University), Håkon Håkonarson(Children's Hospital of Philadelphia), Elizabeth Bhoj(Children's Hospital of Philadelphia), Dong Li(Children's Hospital of Philadelphia), Noriko Miyake(Yokohama City University), Shubha R. Phadke(Sanjay Gandhi Post Graduate Institute of Medical Sciences), Julie Kaylor(University of Arkansas for Medical Sciences), Afifa Irani(Peyton Manning Children’s Hospital at St.Vincent)
Cited by 23
Related Papers
Analysis of shared heritability in common disorders of the brain
|Science|2018|2k
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
|The Lancet|2015|779
Common variants at five new loci associated with early-onset inflammatory bowel disease
|Nature Genetics|2009|483
Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder
|Journal of the American Academy of Child & Adolescent Psychiatry|2010|469