APA
Ji J., Lee H., Argiropoulos B., Dorrani N., Mann J., Martinez-Agosto J. A., Gomez-Ospina N., Gallant N., Bernstein J. A., Hudgins L., Slattery L., Isidor B., Le Caignec C., David A., Obersztyn E., Wiśniowiecka-Kowalnik B., Fox M., Deignan J. L., Vilain E., Hendricks E., Horton Harr M., Noon S. E., Jackson J. R., Wilkens A., Mirzaa G., Salamon N., Abramson J., Zackai E. H., Krantz I., Innes A. M., Nelson S. F., Grody W. W. & Quintero-Rivera F. (20160506). DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. : European journal of human genetics : EJHG.
Chicago
Ji Jianling, Lee Hane, Argiropoulos Bob, Dorrani Naghmeh, Mann John, Martinez-Agosto Julian A, Gomez-Ospina Natalia, Gallant Natalie, Bernstein Jonathan A, Hudgins Louanne, Slattery Leah, Isidor Bertrand, Le Caignec Cédric, David Albert, Obersztyn Ewa, Wiśniowiecka-Kowalnik Barbara, Fox Michelle, Deignan Joshua L, Vilain Eric, Hendricks Emily, Horton Harr Margaret, Noon Sarah E, Jackson Jessi R, Wilkens Alisha, Mirzaa Ghayda, Salamon Noriko, Abramson Jeff, Zackai Elaine H, Krantz Ian, Innes A Micheil, Nelson Stanley F, Grody Wayne W and Quintero-Rivera Fabiola. 20160506. DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. : European journal of human genetics : EJHG.
Harvard
Ji J., Lee H., Argiropoulos B., Dorrani N., Mann J., Martinez-Agosto J. A., Gomez-Ospina N., Gallant N., Bernstein J. A., Hudgins L., Slattery L., Isidor B., Le Caignec C., David A., Obersztyn E., Wiśniowiecka-Kowalnik B., Fox M., Deignan J. L., Vilain E., Hendricks E., Horton Harr M., Noon S. E., Jackson J. R., Wilkens A., Mirzaa G., Salamon N., Abramson J., Zackai E. H., Krantz I., Innes A. M., Nelson S. F., Grody W. W. and Quintero-Rivera F. (20160506). DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. : European journal of human genetics : EJHG.
MLA
Ji Jianling, Lee Hane, Argiropoulos Bob, Dorrani Naghmeh, Mann John, Martinez-Agosto Julian A, Gomez-Ospina Natalia, Gallant Natalie, Bernstein Jonathan A, Hudgins Louanne, Slattery Leah, Isidor Bertrand, Le Caignec Cédric, David Albert, Obersztyn Ewa, Wiśniowiecka-Kowalnik Barbara, Fox Michelle, Deignan Joshua L, Vilain Eric, Hendricks Emily, Horton Harr Margaret, Noon Sarah E, Jackson Jessi R, Wilkens Alisha, Mirzaa Ghayda, Salamon Noriko, Abramson Jeff, Zackai Elaine H, Krantz Ian, Innes A Micheil, Nelson Stanley F, Grody Wayne W and Quintero-Rivera Fabiola. DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. : European journal of human genetics : EJHG. 20160506.