Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

Overview of attention for article published in BMC Medical Genomics, January 2021

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Click to read more: https://t.co/U77gFb78pr #Bione #DNA #ClinicalGenetics #DrChikara For more info visit: https://t.co/S399lcSfAp https://t.co/ujygLwR4je

03 Jul 2021

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Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss. https://t.co/ihJGIVmyHo

23 Jan 2021

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