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Cancer Genetics|March 6, 2022
Detecting the "undetectable" alterations: Use of NGS to uncover high-risk alterationsChelsea Halprin, Sumire Kitahara, Eric Vail, et al.
Cancer Genetics|February 9, 2025
De novo RUNX1-driven acute myeloid leukemia requiring integrative geneticsCeleste C Eno, Jeremy Lorber, Eric Vail, et al.
Cold Spring Harbor Molecular Case Studies|November 18, 2021
Transient myeloproliferative disorder as the presenting feature for mosaic trisomy 21Nicole Baca, Pedro A Sanchez-Lara, Rhona Schreck, et al.
Journal of Visualized Experiments : Jove|May 19, 2017
Functional Manipulation of Maternal Gene Products Using In Vitro Oocyte Maturation in ZebrafishElaine L Welch, Celeste C Eno, Sreelaja Nair, et al.
Molecular Genetics & Genomic Medicine|November 9, 2019
Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centersCeleste C Eno, Stacey K Barton, Naghmeh Dorrani, et al.
American Journal of Medical Genetics. Part A|February 26, 2021
14q32.11 microdeletion including CALM1, TTC7B, PSMC1, and RPS6KA5: A new potential cause of developmental and language delay in three unrelated patientsCeleste C Eno, Jesper Graakjaer, Dea Svaneby, et al.
Current Biology : CB|July 10, 2012
Tropomodulin protects α-catenin-dependent junctional-actin networks under stress during epithelial morphogenesisElisabeth A Cox-Paulson, Elise Walck-Shannon, Allison M Lynch, et al.
Human Genetics|January 3, 2021
5q35 duplication presents with psychiatric and undergrowth phenotypes mediated by NSD1 overexpression and mTOR signaling downregulationFabiola Quintero-Rivera, Celeste C Eno, Christine Sutanto, et al.
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