Coffin–Siris syndrome is a <scp>SWI</scp>/<scp>SNF</scp> complex disorder
Yoshinori Tsurusaki(Yokohama City University), Yoshio Makita(Asahikawa Medical College Hospital), Nobuhiko Okamoto(Osaka Women's and Children's Hospital), Ashwin Dalal(Nizam's Institute of Medical Sciences), Jan Liebelt(South Australia Pathology), Hirofumi Ohashi(Aichi Medical University), Shagun Aggarwal(Nizam's Institute of Medical Sciences), David Mowat(UNSW Sydney), Adila Al‐Kindy(University Hospital of Wales), Bertrand Isidor(Centre National de la Recherche Scientifique), Mitsuko Nakashima(Hamamatsu University School of Medicine), Hirotomo Saitsu(Hamamatsu University), Seiji Mizuno(Aichi Human Service Center), Naomichi Matsumoto(Yokohama City University), Nobuyuki Matsumoto(Asahikawa Medical University), J. Perrier(Nizam's Institute of Medical Sciences), Noriko Miyake(National Center for Global Health and Medicine), M. Fukuda(St. Marianna University School of Medicine)
Cited by 144
Related Papers
Tuberous Sclerosis Complex Diagnostic Criteria Update: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
|Pediatric Neurology|2013|1.5k
Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
|Pediatric Neurology|2013|863
Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort
|Genome biology|2016|404
An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome
|Nature Genetics|1996|385
Diversity and Function of Mutations in P450 Oxidoreductase in Patients with Antley-Bixler Syndrome and Disordered Steroidogenesis
|The American Journal of Human Genetics|2005|348