APA
Mary L., Piton A., Schaefer E., Mattioli F., Nourisson E., Feger C., Redin C., Barth M., El Chehadeh S., Colin E., Coubes C., Faivre L., Flori E., Geneviève D., Capri Y., Perrin L., Fabre-Teste J., Timbolschi D., Verloes A., Olaso R., Boland A., Deleuze J., Mandel J., Gerard B. & Giurgea I. (20190221). Disease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis. : European journal of human genetics : EJHG.
Chicago
Mary Laura, Piton Amélie, Schaefer Elise, Mattioli Francesca, Nourisson Elsa, Feger Claire, Redin Claire, Barth Magali, El Chehadeh Salima, Colin Estelle, Coubes Christine, Faivre Laurence, Flori Elisabeth, Geneviève David, Capri Yline, Perrin Laurence, Fabre-Teste Jennifer, Timbolschi Dana, Verloes Alain, Olaso Robert, Boland Anne, Deleuze Jean-François, Mandel Jean-Louis, Gerard Bénédicte and Giurgea Irina. 20190221. Disease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis. : European journal of human genetics : EJHG.
Harvard
Mary L., Piton A., Schaefer E., Mattioli F., Nourisson E., Feger C., Redin C., Barth M., El Chehadeh S., Colin E., Coubes C., Faivre L., Flori E., Geneviève D., Capri Y., Perrin L., Fabre-Teste J., Timbolschi D., Verloes A., Olaso R., Boland A., Deleuze J., Mandel J., Gerard B. and Giurgea I. (20190221). Disease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis. : European journal of human genetics : EJHG.
MLA
Mary Laura, Piton Amélie, Schaefer Elise, Mattioli Francesca, Nourisson Elsa, Feger Claire, Redin Claire, Barth Magali, El Chehadeh Salima, Colin Estelle, Coubes Christine, Faivre Laurence, Flori Elisabeth, Geneviève David, Capri Yline, Perrin Laurence, Fabre-Teste Jennifer, Timbolschi Dana, Verloes Alain, Olaso Robert, Boland Anne, Deleuze Jean-François, Mandel Jean-Louis, Gerard Bénédicte and Giurgea Irina. Disease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis. : European journal of human genetics : EJHG. 20190221.