Taylor Burt

发表

Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss

B. Fernandez, T. Young, D. O’Rielly, 2019, BMC Medical Genetics.

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

Daniel Vincent, F. Glaser, S. Stanton, 2022, Human Genetics.

Autosomal Dominant Non-Syndromic Hearing Loss Maps to DFNA33 (13q34) and Co-Segregates with Splice Site Variants in ATP11A, A Phospholipid Flippase Gene

Daniel Vincent, S. Stanton, O. Barel, 2021 .

Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses

Daniel Vincent, S. Stanton, T. Young, 2023, European Journal of Human Genetics.