Clinical genetics and therapeutics

370 - Genetic Findings in Patients Presenting with Childhood Apraxia of Speech

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369 - Novel Deleterious ACBD5 Gene Variant Associated with Optic Atrophy, White Matter Disease, and Psychomotor Regression: Case Report and Literature Review

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374 - Molecular Genetic Studies with SNP Arrays and WES in 20 Patients with  Microphthalmia, Anophthalmia and Coloboma (MAC) from Pakistan
375 - CATWOMAN Subtype of Catel-Manzke Syndrome:  Catel-Manzke Syndrome Without Manzke Dysostosis
378 - Clinical Presentation of SMARCA4-Related Coffin-Siris Syndrome – An Additional 29 Cases
381 - Approaches to Secondary Findings Across the Clinical Sequencing Evidence-Generating Research (CSER) Consortium
382 - Elevated Incidence of Microphthalmia in Chuuk, FSM--a Mystery Solved?
383 - A High Carrier Frequency of WFS1 R558C Variant of 2.5%, Associated with Wolfram Syndrome, in the Ashkenazi Jewish Population
386 - The Value of pLI When Disease Mechanism Is Not Well-Established: Classifying LoF Variants in a Clinical Laboratory 
396 - Improved Mapping Quality and Coverage in Highly Homologous PKD1 Gene Enable High Diagnostic Yield in ADPKD
398 - Prenatal and Postnatal 10q24.32 Duplications Detected by SNP microarray
401 - Novel Findings of Craniosynostosis and Horseshoe Kidney Associated with NOG Pathogenic Variant and Stapes Ankylosis with Broad Thumbs and Toes (SABTT)