Expanding the phenotypic spectrum of ARCN1-related syndrome
Alyssa Ritter, Jessica I. Gold, Hiroshi Hayashi, Amanda M. Ackermann, Stephanie Hanke, Cara Skraban, Sanmati Cuddapah, Elizabeth Bhoj, Dong Li, Yukiko Kuroda, Jessica Wen, Ryojun Takeda, Audrey Bibb, Salima El Chehadeh, Amélie Piton, Jeanine Ohl, Mary K. Kukolich, Keisuke Nagasaki, Kohji Kato, Tomoo Ogi, Tricia Bhatti, Pierre Russo, Bryan L. Krock, Jill R. Murrell, Jennifer A. Sullivan, Vandana Shashi, Nicholas Stong, Håkon Håkonarson, Kentaro Sawano, Erin Torti, Rebecca Willaert, Yue Si, William R. Wilcox, Katrine V. Wirgenes, Kristian Thomassen, Katherine Carlotti, Angelika Erwin, Joanna Lazier, Thorsten Marquardt, Miao He, Andrew C. Edmondson, Kosuke Izumi
Topics & Concepts
MicrocephalyCataractsProgeriaMedicineShort staturePediatricsHepatoblastomaIntellectual disabilityPhenotypeIntrauterine growth restrictionInternal medicinePregnancyFetusGeneticsBiologyGeneOphthalmologyPsychiatryGenomics and Rare DiseasesConnective tissue disorders researchNeurological diseases and metabolism