Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2022

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Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III https://t.co/qWxRBu6JMy

22 Feb 2022

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Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III https://t.co/21XuusJ2dp

22 Feb 2022

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Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III https://t.co/hzbxuvBicD https://t.co/VvSkji48kT

22 Feb 2022

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Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III https://t.co/dsOzKYdw7m https://t.co/UWEYLYs5nR

22 Feb 2022

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