Cite
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD
MLA
Granadillo, Jorge Luis, et al. “Pathogenic Variants in TNRC6B Cause a Genetic Disorder Characterised by Developmental Delay/Intellectual Disability and a Spectrum of Neurobehavioural Phenotypes Including Autism and ADHD.” Journal of Medical Genetics, 2020. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1367219849&authtype=sso&custid=ns315887.
APA
Granadillo, J. L., P.A. Stegmann, A., Guo, H., Xia, K., Angle, B., Bontempo, K., Pfundt, R. P., Rosenfeld, J. A., & Shinawi, M. (2020). Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD. Journal of Medical Genetics.
Chicago
Granadillo, Jorge Luis, Alexander P.A. Stegmann, Hui Guo, K. Xia, Brad Angle, Kelly Bontempo, R.P. Pfundt, J.A. Rosenfeld, and M. Shinawi. 2020. “Pathogenic Variants in TNRC6B Cause a Genetic Disorder Characterised by Developmental Delay/Intellectual Disability and a Spectrum of Neurobehavioural Phenotypes Including Autism and ADHD.” Journal of Medical Genetics. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1367219849&authtype=sso&custid=ns315887.