Publications by authors named "Maria Longhurst"

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Validation of MYC and BCL6 rapid break apart digital fluorescence in situ hybridization assays for clinical use.
Michael Liew, Leslie Rowe, Kristina Moore, Emily Aston, Kathryn O'Brien, Maria Longhurst

Int J Clin Exp Pathol· April 2023

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Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p Mosaicism.
Reha M Toydemir, Emanuele Panza, Maria C Longhurst, Sarah T South, Alan F Rope

Mol Syndromol· July 2020

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A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay.
Prabakaran Paulraj, Michelle Bosworth, Maria Longhurst, Callie Hornbuckle, Garrett Gotway

Cytogenet Genome Res· December 2019

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Pediatric acute myeloid leukemia with t(7;21)(p22;q22).
Prabakaran Paulraj, Steven Diamond, Faisal Razzaqi, J Daniel Ozeran, Maria Longhurst

Genes Chromosomes Cancer· August 2019

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Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumors.
John C Herriges, Sara Brown, Maria Longhurst, Jillian Ozmore, John B Moeschler

Eur J Med Genet· January 2019

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Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing.
Wei Shen, Christian N Paxton, Philippe Szankasi, Maria Longhurst, Jonathan A Schumacher

J Clin Pathol· April 2018

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Braddock-Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1.
Stephen R Braddock, Sarah T South, Joshua D Schiffman, Maria Longhurst, Leslie R Rowe

Am J Med Genet A· October 2016

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