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1. Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease

2. Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases

3. Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases

4. A clinical laboratory's experience using GeneMatcher—Building stronger gene–disease relationships

5. Tracing nonlegume orthologs of legume genes required for nodulation and arbuscular mycorrhizal symbioses

6. Tracing Nonlegume Orthologs of Legume Genes Required for Nodulation and Arbuscular Mycorrhizal Symbioses.

7. The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships.

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