Laboratory genetics and genomics

668 - A retrospective study of 97 array comparative genomic hybridization cases with recurrent and nonrecurrent genomic rearrangements at 15q11-q13

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667 - Expanding the Genetic Spectrum of Cerebral Palsy: Trio Whole Genome Sequencing of 38 Families Identifies Genetic Causes in 18 Different Genes

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669 - Is Likely Pathogenic Really 90% Likely? A Look at the Data
670 - Leveraging 4,697 Reconstructed Pedigrees from 92k Exomes Identifies De Novo and Rare Segregating Disease-Causing Mutations in Families
674 - The Utility of Whole Exome Sequencing in a Pediatric Intensive Care Unit
675 - A Retrospective Study Based On > 167K Fragile X Female Carrier Screening Cases
682 - Standards for the Classification and Reporting of Constitutional Copy Number Variants: A ClinGen/ACMG Joint Consensus Recommendation
683 - Preliminary Results of SouthSeq: Sequencing NICU Newborns in the South
685 - Maintaining Sample Provenance: How Inclusion of Routine Genotyping Improves the Quality of Patient Results
687 - Impact of Familial Communication on Relatives in Patient-Driven Studies for Reclassification of Variants of Uncertain Significance
692 - By the Way: The Incidental Benefit of Exome Sequencing to Enable Life-Saving Intervention via Secondary Findings
702 - Harmonizing clinical interpretation of intragenic sequence and copy number variants in monogenic disease