William Ross Wilcox (William R Wilcox)

Publication Activity (10 Years)

Years Active: 2016-2022
Publications (10 Years): 3

Top Topics

Mitochondrial Dna

Hypertrophic Cardiomyopathy

High Throughput

Top Venues

American journal of medical genetics. Part C, Seminars in medical genetics

Genetics in medicine : official journal of the American College of Medical Genetics

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

Publications

Patricia Liane Hall, Angela Lynn Wittenauer, William Ross Wilcox
Proximal urea cycle defects are challenging to detect with newborn screening: Results of a prospective pilot study using post-analytical tools. American journal of medical genetics. Part C, Seminars in medical genetics 190 (2) (2022)
Kathryn Elkins, Angela Lynn Wittenauer, Arthur F Hagar, Rachel Logan, Elizabeth Sekul, Yijin Xiang, Sumit Verma, William Ross Wilcox
Georgia state spinal muscular atrophy newborn screening experience: Screening assay performance and early clinical outcomes. American journal of medical genetics. Part C, Seminars in medical genetics 190 (2) (2022)
Elfrida R Benjamin, Maria Cecilia Della Valle, Xiaoyang Wu, Evan Katz, Farhana Pruthi, Sarah Bond, Benjamin Bronfin, Hadis Williams, Julie Yu, Daniel G Bichet, Dominique Paul Germain, Roberto Giugliani, Derralynn A Hughes, Raphael Schiffmann, William Ross Wilcox, Robert J Desnick, John Kirk, Jay Barth, Carrolee Barlow, Kenneth J Valenzano, Jeff Castelli, David J Lockhart
The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastat. Genetics in medicine : official journal of the American College of Medical Genetics 19 (4) (2016)