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RT @FrontGenetics: New Research: Case Report: A Novel Gross Deletion in PAX3 (10.26 kb) Identified in a Chinese Family With Waardenburg Syn…
RT @FrontGenetics: New Research: Case Report: A Novel Gross Deletion in PAX3 (10.26 kb) Identified in a Chinese Family With Waardenburg Syn…
New Research: Case Report: A Novel Gross Deletion in PAX3 (10.26 kb) Identified in a Chinese Family With Waardenburg Syndrome by Third-Generation Sequencing: Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with… https://t.c