Clinical genetics and therapeutics

358 - Co-occurrence of Duchenne Muscular Dystrophy and Klinefelter’s Syndrome-A Modified Phenotype

Previous Eposter
356 - Novel Comorbidities and Natural History Analysis of the 17q21.31 Microdeletion Syndrome (KdVS) Through GenIDA, a Participatory International Online Database for Genetic Forms of Intellectual Disability and Autism

Next Eposters
359 - Novel DOCK7 Pathogenic Variants in Three Siblings with Epileptic Encephalopathy, Cortical Visual Impairment, and Structural Brain Abnormalities
360 - The clinical features and genotypes of neurofibromatosis type 1 patients with NF1 microdeletions
363 - Natural History of Achondroplasia: a Retrospective Study of Patients Managed by a Multispecialty Program.
368 - Oral Chelation Therapy to Treat HypermanganesemiaOral Chelation Therapy to Treat Hypermanganesemia
369 - Novel Deleterious ACBD5 Gene Variant Associated with Optic Atrophy, White Matter Disease, and Psychomotor Regression: Case Report and Literature Review
370 - Genetic Findings in Patients Presenting with Childhood Apraxia of Speech
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