Case report: A novel mutation in TRPS1 identified in a Chinese family with tricho-rhino-phalangeal syndrome I: A therapeutic challenge

Overview of attention for article published in Frontiers in Pediatrics, November 2022

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New Research: Case report: A novel mutation in TRPS1 identified in a Chinese family with tricho-rhino-phalangeal syndrome I: A therapeutic challenge: Tricho-rhino-phalangeal syndrome (TRPS) is a rare autosomal dominant malformation caused by… https://t.co/

24 Dec 2022

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