Publications by authors named "Erin Royer"

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The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.
Dmitrijs Rots, Taryn E Jakub, Crystal Keung, Adam Jackson, Siddharth Banka, Erin Royer

Am J Hum Genet· November 2025

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The impact of clinical genome sequencing in a global population with suspected rare genetic disease.
Erin Thorpe, Taylor Williams, Chad Shaw, Evgenii Chekalin, Julia Ortega, Erin Royer

Am J Hum Genet· July 2024

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The smallest likely pathogenic duplication of a SOX9 enhancer identified to date in a family with 46,XX testicular differences of sex development.
Samin A Sajan, Carolyn M Brown, Laura Davis-Keppen, Kaitlyn Burns, Erin Royer

Am J Med Genet A· December 2023

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The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.
Dmitrijs Rots, Taryn E Jakub, Crystal Keung, Adam Jackson, Siddharth Banka, Erin Royer

Am J Hum Genet· June 2023

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