Eyes on CHARGE syndrome: Roles of CHD7 in ocular development

por Krueger, Laura A., Morris, Ann C.
Publicado 2022

Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1

por Ahmed, Mariya R., Sethna, Saumil, Krueger, Laura A., Yang, Michael B., Hufnagel, Robert B.
Publicado 2022

Her9/Hes4 is required for retinal photoreceptor development, maintenance, and survival

por Coomer, Cagney E., Wilson, Stephen G., Titialii-Torres, Kayla F., Bills, Jessica D., Krueger, Laura A., Petersen, Rebecca A., Turnbaugh, Evelyn M., Janesch, Eden L., Morris, Ann C.
Publicado 2020

Author Correction: Her9/Hes4 is required for retinal photoreceptor development, maintenance, and survival

por Coomer, Cagney E., Wilson, Stephen G., Titialii-Torres, Kayla F., Bills, Jessica D., Krueger, Laura A., Petersen, Rebecca A., Turnbaugh, Evelyn M., Janesch, Eden L., Morris, Ann C.
Publicado 2020

Mutations in the UGO1-like protein SLC25A46 cause an optic atrophy spectrum disorder

por Abrams, Alexander J., Hufnagel, Robert B., Rebelo, Adriana, Zanna, Claudia, Patel, Neville, Gonzalez, Michael A., Campeanu, Ion J., Griffin, Laurie B., Groenewald, Saskia, Strickland, Alleene V., Tao, Feifei, Speziani, Fiorella, Abreu, Lisa, Schüle, Rebecca, Caporali, Leonardo, La Morgia, Chiara, Maresca, Alessandra, Liguori, Rocco, Lodi, Raffaele, Ahmed, Zubair M., Sund, Kristen L., Wang, Xinjian, Krueger, Laura A., Peng, Yanyan, Prada, Carlos E., Prows, Cynthia A., Bove, Kevin, Schorry, Elizabeth K., Antonellis, Anthony, Zimmerman, Holly H., Abdul-Rahman, Omar A., Yang, Yaping, Downes, Susan M., Prince, Jeffery, Fontanesi, Flavia, Barrientos, Antonio, Nemeth, Andrea H., Carelli, Valerio, Huang, Taosheng, Zuchner, Stephan, Dallman, Julia E.
Publicado 2015