Ιατρικά Άρθρα Αλέξανδρος Γ. Σφακιανάκης: Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling

Κυριακή 21 Ιανουαρίου 2018

Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling

To identify the pathogenic mutation and provide prenatal counseling and diagnosis in two large Chinese families with autosomal dominant all-frequency hearing loss.

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Ιατρικά Άρθρα Αλέξανδρος Γ. Σφακιανάκης

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Κυριακή 21 Ιανουαρίου 2018

Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling

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