Clinical genetics and therapeutics

274 - Two-Year Real-World Effectiveness of Oral Eliglustat in Treatment-Naïve and Switch Patients Enrolled in the International Collaborative Gaucher Group Gaucher Registry

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272 - Concordance Analysis on Products of Conception Samples Reveals Monozygotic Twin Gestations with Discrepant Chromosome Findings

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277 - DEVELOPMENTAL GENOME ANATOMY PROJECT (DGAP): A two decades hub for gene discovery and the flourishing of sequencing in cytogenetics
278 - Evaluation of a Phenotyping App in the Detection of Known Genetic Disorders
280 - Phenotypic spectrum associated with mutations of PGAP2 in hyperphosphatasia with mental retardation syndrome-3 (HPMRS3) Mabry syndrome (OMIM 239300).
281 - Retrospective Electronic Medical Record Analysis Identifies Subjects at Risk of Hypophosphatasia; High Proportion with Concurrent Autoimmune/Endocrine Diagnoses
288 - Preliminary Insight from CADASIL Testing: Using Aggregate Patient Data to Correlate Position of Variants in NOTCH3 to Severity of Disease
291 - Roberts Individualized Medical Genetics Center Hearing Loss Clinic Experience 
294 - ClinGen’s Variant Prioritization Tool (VPT): A Tool for Prioritizing Clinical Variants at Scale
295 - Precision Medicine Advancements Using Whole Genome Sequencing, Noninvasive Whole Body Imaging, and Functional Diagnostics
298 - The Majority of Index Patients with Vascular Ehlers-Danlos Syndrome Do not Have a Positive Family History  
299 - Correlations between Glucosylsphingosine (Lyso-GL-1) and Disease Severity and Response to Oral Eliglustat in Treatment-Naïve Adults with Gaucher Disease Type 1