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Brain & Development|January 29, 2023
A novel splice site CUL3 variant in a patient with neurodevelopmental delayKrista M Vincent, Danielle K Bourque
Archives of Oral Biology|November 6, 2020
The solubility of calcium oxalates explains some aspects of their underrepresentation in the oral cavityKrista M Vincent, Paul V Azzopardi, Silvia Mittler, et al.
European Journal of Medical Genetics|April 3, 2025
Familial inheritance of 14q terminal deletion syndrome and review of the literatureKrista M Vincent, Bradley Prince, Jean McGowan-Jordan, et al.
Plos One|April 19, 2016
A Digital PCR-Based Method for Efficient and Highly Specific Screening of Genome Edited CellsScott D Findlay, Krista M Vincent, Jennifer R Berman, et al.
The Journal of Investigative Dermatology|July 14, 2015
CCN2 Expression by Tumor Stroma Is Required for Melanoma MetastasisJames Hutchenreuther, Krista M Vincent, David E Carter, et al.
Molecular Genetics & Genomic Medicine|March 14, 2022
Expanding the clinical spectrum of autosomal-recessive renal tubular dysgenesis: Two siblings with neonatal survival and review of the literatureKrista M Vincent, Afrah Alrajhi, Joanna Lazier, et al.
Clinical Genetics|August 9, 2021
Delineating the expanding phenotype of HERC2-related disorders: The impact of biallelic loss of function versus missense variationKrista M Vincent, Alison Eaton, Vahid Reza Yassaee, et al.
American Journal of Medical Genetics. Part A|June 4, 2025
Ocular Findings as the Most Striking Manifestation of a SMAD3 VariantNoémie Villeneuve-Cloutier, Christie A Boswell-Patterson, Lucas Bronicki, et al.
Cancer Research Communications|February 16, 2024
Cancer-associated Fibroblast-specific Expression of the Matricellular Protein CCN1 Coordinates Neovascularization and Stroma Deposition in Melanoma MetastasisJames Hutchenreuther, John Nguyen, Katherine Quesnel, et al.
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