U2AF1(S34/Q157) Variants Detected in cis Arise Sequentially in an MDS Patient With Serial Sequencing Spanning 18 Years

por Ferrone, Christina K., McNaughton, Amy J. M., Vincelli, Felicia, Zuzarte, Philip, Lee, David, Feilotter, Harriet E., Rauh, Michael J.
Publicado 2022

De novo duplication on Chromosome 19 observed in nuclear family displaying neurodevelopmental disorders

por Sjaarda, Calvin P., Kaiser, Beatrice, McNaughton, Amy J.M., Hudson, Melissa L., Harris-Lowe, Liam, Lou, Kyle, Guerin, Andrea, Ayub, Muhammad, Liu, Xudong
Publicado 2020

Interplay between maternal Slc6a4 mutation and prenatal stress: a possible mechanism for autistic behavior development

por Sjaarda, Calvin P., Hecht, Patrick, McNaughton, Amy J. M., Zhou, Audrina, Hudson, Melissa L., Will, Matt J., Smith, Garth, Ayub, Muhammad, Liang, Ping, Chen, Nansheng, Beversdorf, David, Liu, Xudong
Publicado 2017