APA
Thevenon J., Callier P., Thauvin-Robinet C., Mejean N., Falcon-Eicher S., Maynadie M., de Maistre E., Bidot S., Huet F., Beri-Dexheimer M., Jonveaux P., Mugneret F. & Faivre L. (20110517). De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection. : American journal of medical genetics. Part A.
Chicago
Thevenon Julien, Callier Patrick, Thauvin-Robinet Christel, Mejean Nathalie, Falcon-Eicher Sylvie, Maynadie Marc, de Maistre Emmanuel, Bidot Samuel, Huet Frédéric, Beri-Dexheimer Mylène, Jonveaux Philippe, Mugneret Francine and Faivre Laurence. 20110517. De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection. : American journal of medical genetics. Part A.
Harvard
Thevenon J., Callier P., Thauvin-Robinet C., Mejean N., Falcon-Eicher S., Maynadie M., de Maistre E., Bidot S., Huet F., Beri-Dexheimer M., Jonveaux P., Mugneret F. and Faivre L. (20110517). De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection. : American journal of medical genetics. Part A.
MLA
Thevenon Julien, Callier Patrick, Thauvin-Robinet Christel, Mejean Nathalie, Falcon-Eicher Sylvie, Maynadie Marc, de Maistre Emmanuel, Bidot Samuel, Huet Frédéric, Beri-Dexheimer Mylène, Jonveaux Philippe, Mugneret Francine and Faivre Laurence. De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection. : American journal of medical genetics. Part A. 20110517.