Clinical genetics and therapeutics

597 - Deletion 2q22.1q22.3: An Emerging Microdeletion Syndrome with Variable Phenotype

Previous Eposter
596 - The INCLUDE (INvestigation of Co-occurring conditions across the Lifespan to Understand Down syndromE) Project for Down Syndrome Research at NIH

Next Eposters
601 - Single Family Case Report: Germline mosaicism in nevoid basal cell carcinoma syndrome (NBCCS)
602 - A Unique Case of Mosaic Turner Syndrome and Partial Trisomy 17p
604 - Coexistence of monosomy 21 and trisomy 15: effects of genomic imbalance
606 - Severe Dilated Cardiomyopathy in a Patient with Cardiospondylocarpofacial Syndrome with MAP3K7 Variant
613 - Genetic Counseling and Returning Negative Genomic Screening Results in Large Cohorts: Findings from the RAVE Study
614 - Lifetime Risk of Breast Cancer from Polygenic Risk Scores Combined with Clinical Assessment in Women Referred for Genetic Testing
624 - The Effect of Family Study of Co-Segregation Analysis on Outcome of Multi-Gene Panel Sequencing Test Result.
625 - Genetic Counseling and Testing in Patients with Prior Germline Testing: Experience of Community Sites for a Major Cancer Center
627 - Family History of Autism Spectrum Disorder in the Prenatal Genetic Counseling Session
629 - Is Bigger Always Better? Managing Expanding Genotype Phenotypes Correlations with Multi-Gene Hereditary Cancer Panels