Publications by authors named "Brady Slater"

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Phenotypic Expansion of Autosomal Dominant SREBF1-Related Ichthyosis Follicularis, Atrichia, Photophobia: It Is in Fact the Same Condition as Hereditary Mucoepithelial Dysplasia.
Brady A Slater, Samantha Seymour, Emma Burt, Janell Kierstein, Austin A Larson

Clin Genet· January 2026

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Health-related quality of life in adults with osteogenesis imperfecta.
Chaya N Murali, Brady Slater, Salma Musaad, David Cuthbertson, Dianne Nguyen

Clin Genet· June 2021

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Sudden infant death with dysgenesis of the testes syndrome in a non-Amish infant: A case report.
Brady Slater, Kevin Glinton, Hongzheng Dai, Erica Lay, Lefkothea Karaviti

Am J Med Genet A· November 2020

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Pediatric Outcomes Data Collection Instrument is a Useful Patient-Reported Outcome Measure for Physical Function in Children with Osteogenesis Imperfecta.
Chaya N Murali, David Cuthbertson, Brady Slater, Dianne Nguyen, Alicia Turner

Genet Med· March 2020

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Nephronophthisis due to a novel DCDC2 variant in a patient from African-Caribbean descent: A case report.
Brady Slater, Nasim Bekheirnia, Joseph Angelo, Weimen Bi, Michael C Braun

Am J Med Genet A· March 2020

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