Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. | UCSF Helen Diller Family Comprehensive Cancer Center

Author List

Zarate YA, Perry H, Ben-Omran T, Sellars EA, Stein Q, Almureikhi M, Simmons K, Klein O, Fish J, Feingold M, Douglas J, Kruer MC, Si Y, Mao R, McKnight D, Gibellini F, Retterer K, Slavotinek A

Publication

American journal of medical genetics. Part A

Publication ID (Profile URL)

https://researcherprofiles.org/profile/1190627

Publication Year

2015

PubMed ID

25885067

Publication Title

Zarate YA, Perry H, Ben-Omran T, Sellars EA, Stein Q, Almureikhi M, Simmons K, Klein O, Fish J, Feingold M, Douglas J, Kruer MC, Si Y, Mao R, McKnight D, Gibellini F, Retterer K, Slavotinek A. Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. Am J Med Genet A. 2015 May; 167A(5):1026-32.