Mary E. Brunkow

[Table, GeneReview Scope].

Peter Beighton, Herman Hamersma, Mary E. Brunkow, 2013 .

A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA→AAUGAA) leads to the IPEX syndrome

Hans D. Ochs, Mary E. Brunkow, H. Ochs, 2001, Immunogenetics.

Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

Jared C. Roach, Gustavo Glusman, Fengfeng Zhou, 2015, PloS one.

Identification of copy number variants in whole-genome data using Reference Coverage Profiles

Jared C. Roach, Gustavo Glusman, Max Robinson, 2015, Front. Genet..