Clinical Findings Associated with a De Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis by Omid Kohannim, Jane Peredo, Katrina M. Dipple, Fabiola Quintero-Rivera

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Outcomes of two different unbalanced segregations from a maternal t(4;10)(q33;p15.1) translocation by Judith Fan, T. Niroshini Senaratne, Jason Y. Liu, Michelle Bina, Julian A. Martinez-Agosto, Fabiola Quintero-Rivera, Jessica J. Wang

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P836: A framework and implementation of the Association of Professors of Human and Medical Genetics updated core competencies for medical school by Fabiola Quintero-Rivera, Sabrina Nuñez, Jonathan Bernstein, David Gardner, Aditi Parikh, Erin Strovel, Myla Ashfaq, Renee LeClair, Lauren Massingham

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P109: Identification of new fusion partners for ETV6 gene in hematologic malignancy by next generation sequencing (NGS) by Sumayya Aslam, Nyein Nyein Htun, Piyanuch Kongtim, Kiran Naqvi, Deepa Jeyakumar, Xiaohui Zhao, Sherif Rezk, Fabiola Quintero-Rivera, Jefferson Chan, Ying Zhang

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P091: Unfavorable disease progression in patients with chronic myeloid leukemia and concurrent t(6;9) translocation (DEK-NUP214 fusion) or inversion 16 by Ying Zhang, Jack Reid, Kapitolina Semenova, Deepa Jeyakumar, Lisa Lee, Katherine Dang, Johnson Tso, Lynn Yang, Angela Fleishman, Jefferson Chan, Xiaohui Zhao, Fabiola Quintero-Rivera

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O34: Application of long-read sequencing and telomere-to-telomere genome assembly unveils complex rearrangements and cryptic breakpoints of Robertsonian translocation and ring chro... by Fabiola Quintero-Rivera, Yulia Mostovoy, Philip Boone, Steve Huang, Kiran Garimella, Julian Martinez-Agosto, Bianca Russell, Tera Bowers, Tim De Smet, Stacey Gabriel, James Gusella, Harrison Brand, Michael Talkowski

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O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions by Courtney Verscaj, Frances Velez-Bartolomei, Ethan Bodle, Katie Chan, Michael Lyons, Willa Thorson, Wen-Hann Tan, John Graham, Angela Peron, Fabiola Quintero-Rivera, Elaine Zackai, Mary Ann Thomas, Cathy Stevens, Margaret Adam, Lynne Bird, Marilyn Jones, Dena Matalon

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Increased AID results in mutations at the CRLF2 locus implicated in Latin American ALL health disparities by Valeria Rangel, Jason N. Sterrenberg, Aya Garawi, Vyanka Mezcord, Melissa L. Folkerts, Sabrina E. Calderon, Yadhira E. Garcia, Jinglong Wang, Eli M. Soyfer, Oliver S. Eng, Jennifer B. Valerin, Sora Park Tanjasiri, Fabiola Quintero-Rivera, Marcus M. Seldin, Selma Masri, Richard L. Frock, Angela G. Fleischman, Nicholas R. Pannunzio

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