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Additional file 1 of Whole-exome sequencing identifies a de novo PDE3A variant causing autosomal dominant hypertension with brachydactyly type E syndrome: a case report

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posted on 2020-07-07, 05:02 authored by Xianqing Li, Zongzhe Li, Peng Chen, Yan Wang, Dao Wen Wang, Dao Wu Wang
Additional file 1: Figure S1. Illustration for the filtering process of WES. (PPTX 39 kb)

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National Natural Science Foundation of China National Key R&D Program of China National Key R&D Program of China

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    BMC Medical Genetics

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    HypertensionBrachydactylyHypertension with brachydactyly type E syndromeWhole-exome sequencingGenetic diagnosis

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