APA

García-Ortiz J. E., Zarazúa-Niño A. I., Hernández-Orozco A. A., Reyes-Oliva E. A., Pérez-Ávila C. E., Becerra-Solano L. E., Galán-Huerta K. A., Rivas-Estilla A. M. & Córdova-Fletes C. (062020). Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder. : Journal of autism and developmental disorders.

Chicago

García-Ortiz José E, Zarazúa-Niño Ana I, Hernández-Orozco Angélica A, Reyes-Oliva Edwin A, Pérez-Ávila Carlos E, Becerra-Solano Luis E, Galán-Huerta Kame A, Rivas-Estilla Ana M and Córdova-Fletes Carlos. 062020. Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder. : Journal of autism and developmental disorders.

Harvard

García-Ortiz J. E., Zarazúa-Niño A. I., Hernández-Orozco A. A., Reyes-Oliva E. A., Pérez-Ávila C. E., Becerra-Solano L. E., Galán-Huerta K. A., Rivas-Estilla A. M. and Córdova-Fletes C. (062020). Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder. : Journal of autism and developmental disorders.

MLA

García-Ortiz José E, Zarazúa-Niño Ana I, Hernández-Orozco Angélica A, Reyes-Oliva Edwin A, Pérez-Ávila Carlos E, Becerra-Solano Luis E, Galán-Huerta Kame A, Rivas-Estilla Ana M and Córdova-Fletes Carlos. Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder. : Journal of autism and developmental disorders. 062020.