Search Results - Zoe Lewis
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P500: Reinterpretation of postnatal clinical copy number variants: A practical approach for implementation as a routine laboratory practice by Zoe Lewis, Daniel Reich, Timothy Tidwell, Benjamin Clyde, Scott Zobell, Denise Quigley, Erica Andersen
Published in Genetics in Medicine Open (2023-01-01)Get full text
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P536: 2q11.2 recurrent CNVs including TMEM127: A collaborative multi-center study to expand knowledge of neurodevelopmental phenotypes and pheochromocytoma/paraganglioma syndrome p... by Lucilla Pizzo, Zoe Lewis, Lauren Walsh, Cassandra Runke, Margit Nõukas, Katrin Männik, Neeme Tõnisson, Erik Thorland, Christa Martin, Katie Rudd, Erica Andersen
Published in Genetics in Medicine Open (2023-01-01)Get full text
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P603: Utility of cytogenomic SNP microarray for bone marrow failure syndrome patients by Lucilla Pizzo, Jian Zhao, Adam Clayton, Julie Feusier, Coumarane Mani, Zoe Lewis, Rachel Lasher, Denise Quigley, Katharine Rudd, Erica Andersen, Bo Hong
Published in Genetics in Medicine Open (2024-01-01)Get full text
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P485: Evaluating novel dosage sensitivity predictors for inclusion in the classification of recurrent copy number variants by John Herriges, Cassandra Runke, Zoe Lewis, Lucilla Pizzo, Bradley Coe, Laura Conlin, Benjamin Hilton, Brynn Levy, Andrea Vaags, Shulin Zhang, Christa Martin, Erica Andersen
Published in Genetics in Medicine Open (2023-01-01)Get full text
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P657: NSD2 duplication results in distinct phenotype and DNA methylation signature by Benjamin Hilton, Bekim Sadikovic, Alfredo Brusco, Giovanni Battista Ferrero, Barbara DuPont, Matthew Tedder, Raymond Louie, Nikhil Sahajpal, Erica Andersen, Zoe Lewis, Amanda Openshaw, Jennifer Kerkhof, Haley McConkey, Raissa Relator, Sadegheh Haghshenas, Jack Reilly, Kathleen Rooney
Published in Genetics in Medicine Open (2023-01-01)Get full text
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