P406: A novel UBA2 variant causing aplasia cutis congenita with ectrodactyly skeletal (ACCES) syndrome in a family with variable expressivity by Nathaniel Jensen, Alexa Dickson, Molly Schroeder, Katherine King

Get full text

P872: Incidental detection of a 33.8Mb maternal Xq deletion during prenatal screening: A case presentation by Hamed Rahi, Yang Cao, Jeffrey Dicke, Amie Stanley, Molly Schroeder, Katarzyna Polonis

Get full text

Qualitative application of the RE-AIM/PRISM framework to an educational intervention for improving the care of persons with behavioral and psychological symptoms of dementia by Tamara J. LeCaire, Molly Schroeder, Uriel Paniagua, Jonathan Stone, Tammi Albrecht, Stephanie L. Houston, Sarina B. Schrager, Cynthia M. Carlsson, Art Walaszek

Get full text

P715: Testing indications and diagnostic yield of clinical exome sequencing in a US Midwestern patient cohort by Michelle Thompson, Mathues Vernet Machado Bressan Wilke, Alexa Dickson, Meagan Corliss, Katarzyna Thompson, Yang Cao, Gregory Spencer, Jason Walker, Kilannin Krysiak, Patricia Dickson, Kevin Bowling, Julie Neidich, Molly Schroeder

Get full text