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Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients.
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has major subject area list
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Rare Diseases; Undiagnosed Diseases
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information resource reference
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McQuerry JA, Mclaird M, Hartin SN, Means JC, Johnston J, Pastinen T, Younger ST. Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients. Sci Rep. 2022 05 09; 12(1):7576.
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label
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Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients.
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