Clinical genetics and therapeutics

303 - Genetic Identification of Lysosomal Storage Disorders in a Multi-Ethnic Biobank

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302 - Growth Hormone Deficiency: Expanding the Phenotype of Potocki-Lupski syndrome

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305 - CSNK2B: A Novel Cause of Neurodevelopmental Disease and Epilepsy
310 - The Importance of Assessing for Triploidy Beyond the First Trimester of Pregnancy
318 - Novel EIF2S3 Missense Mutation in a Large Family with MEHMO Syndrome
319 - The Use and Potential Impact of Diversity Measures in Medical Genetics Practice: Results of a Survey of Clinical Genomics Professionals
329 - Development of concurrent pre-implantation genetic testing for single gene disorders and aneuploidy screening from a single trophectoderm (TE) biopsy using targeted next generation sequencing (NGS)
330 - Analytical validation and chromosomal distribution of regions of homozygosity by oligonucleotide array comparative genomic hybridization from normal prenatal and postnatal case series
331 - Cardiomyopathy in children with mitochondrial disease: prognosis and genetic background
332 - Genetic Testing in an Unselected HCM Cohort: A Descriptive Overview
334 - Migalastat Reduces Globotriaosylceramide (GL-3) Inclusions in Renal Peritubular Capillaries in Patients With Fabry Disease: Post hoc Analyses from FACETS
337 - Compound Heterozygous Variants in IL6ST Associated with Immunodeficiency and GP130 Deficiency