Familial Pediatric Clear Cell Meningioma With Germline SMARCE1 Mutation in the United States

por Navalkele, Pournima, Guzman, Miguel, Kirby, Amelia, Pinz, Hailey, Kemp, Joanna
Publicado 2020

Hirschsprung Disease in an Infant with L1 syndrome: Report of a New Case and a novel L1CAM variant

por Gauntner, Timothy D., Karumuri, Manasa, Guzman, Miguel A., Starnes, Sara E., Besmer, Sherri, Pinz, Hailey, Braddock, Stephen R., Andreone, Teresa L.
Publicado 2021

Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1

por Johnson, Tyler B., Mechels, Keegan, Anderson, Ruth Ellen, Cain, Jacob T., Sturdevant, David A., Braddock, Stephen, Pinz, Hailey, Wilson, Mark A., Landsverk, Megan, Roux, Kyle J., Weimer, Jill M.
Publicado 2018

Author Correction: Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1

por Johnson, Tyler B., Mechels, Keegan, Anderson, Ruthellen H., Cain, Jacob T., Sturdevant, David A., Braddock, Stephen, Pinz, Hailey, Wilson, Mark A., Landsverk, Megan, Roux, Kyle J., Weimer, Jill M.
Publicado 2020