Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care
Rossana Sanchez Russo, Michael J. Gambello, Melissa M. Murphy, Katrina Aberizk, Emily Black, T. Lindsey Burrell, Grace Carlock, Joseph F. Cubells, Michael T. Epstein, Roberto España, Katrina Goines, Ryan M. Guest, Cheryl Klaiman, Sookyong Koh, Elizabeth J. Leslie, Longchuan Li, Derek M. Novacek, Celine A. Saulnier, Esra Sefik, Sarah Shultz, Elaine F. Walker, Stormi P. White, Hallie Averbach, Gary J. Bassell, Shanthi Cambala, Tamara Caspary, David J. Cutler, Paul A. Dawson, Michael P. Epstein, H. Richard Johnston, Bryan C. Mak, Tamika Malone, Trenell J. Mosley, Ava Papetti, Rebecca M. Pollak, Ryan H. Purcell, Nikisha Sisodoya, Steven A. Sloan, Stephen T. Warren, David Weinshenker, Zhexing Wen, Mike Zwick, Jennifer G. Mullé
Topics & Concepts
MedicinePsychosisNeuroimagingAutism spectrum disorderPsychiatryNeurodevelopmental disorderReferralProdromeAnxietyIntellectual disabilityPediatricsAutismFamily medicineGenomic variations and chromosomal abnormalitiesCongenital heart defects researchGenomics and Rare Diseases