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Kate Mowrey

Years Active: 2020-2022
Publications (10 Years): 5

University of Texas Health Science Center at Houston

University of Texas Health Science Center at Houston (MSC)

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

Affiliation History

University of Texas Health Science Center at Houston Jun 18o 2018

United States

Genetic Counselor :: Pediatrics

Education History

University of Texas Health Science Center at Houston Aug 1o 2016

United States

MSC

Publications

Elizabeth Langley, Laura S Farach, Mary K Koenig, Hope Northrup, David F Rodriguez-Buritica, Kate Mowrey
NEXMIF pathogenic variants in individuals of Korean, Vietnamese, and Mexican descent. American journal of medical genetics. Part A 188 (6) (2022)
Mariana Lopez Martinolich, Hope Northrup, Pedro Mancias, Paul R Hillman, Kavya Indira Rao, Kate Mowrey
Identification of a novel microdeletion causative of Nance-Horan syndrome. Molecular genetics & genomic medicine 10 (3) (2022)
Kathryn A Gunther, Kate Mowrey, Laura Schoch Farach
Two new reported cases of 16q22.3q23.3 duplication syndrome highlight intrafamilial variability and potential sex expression differences within a rare duplication syndrome. Clinical case reports 9 (3) (2021)
Stuart M Fraser, Mary Koenig, Laura Farach, Pedro Mancias, Kate Mowrey
A De Novo case of autosomal dominant mitochondrial membrane protein-associated neurodegeneration. Molecular genetics & genomic medicine 9 (7) (2021)
Kate Mowrey, Mary Kay Koenig, Charles Ákos Szabo, Joshua A Samuels, Shannon Mulligan, Deborah A Pearson, Hope Northrup
Two different genetic etiologies for tuberous sclerosis complex (TSC) in a single family. Molecular genetics & genomic medicine 8 (7) (2020)

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