Additional file 3 of Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
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https://springernature.figshare.com/articles/dataset/Additional_file_3_of_Integration_of_whole_genome_sequencing_into_a_healthcare_setting_high_diagnostic_rates_across_multiple_clinical_entities_in_3219_rare_disease_patients/14228419/1
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Additional file 3: Table S7. List of genes and variants reported in cases.
提供机构：
Ann-Charlotte Wikström; Ellika Sahlin; Britt-Marie Anderlid; Giedre Grigelioniene
创建时间：
2021-03-17
