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1. Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder loci

3. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

4. Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

5. Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

6. Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

7. Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome

8. High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

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