Daniel C Koboldt

Years Active: 2020-2021
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Marilena Melas, Esko A Kautto, Samuel J Franklin, Mari Mori, Kim L McBride, Theresa Mihalic Mosher, Ruthann B Pfau, Maria Elena Hernandez-Gonzalez, Sean D McGrath, Vincent J Magrini, Peter White, Julie Balch Samora, Daniel C Koboldt, Richard K Wilson
Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactyly. Human mutation (2021)
Daniel C Koboldt, Megan A Waldrop, Richard K Wilson, Kevin M Flanigan
The Genotypic and Phenotypic Spectrum of BICD2 Variants in Spinal Muscular Atrophy. Annals of neurology 87 (4) (2020)

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