Publications by authors named "Corrine Fillman"

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Combining clinical and molecular characterization of CDH1: a multidisciplinary approach to reclassification of a splicing variant.
Corrine Fillman, Arravinth Anantharajah, Briana Marmelstein, Monica Dillon, Carolyn Horton

Fam Cancer· October 2023

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A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome.
Stuart Baker, Carol Booth, Corrine Fillman, Michael Shapiro, Michael P Blair

Am J Med Genet A· July 2011

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