Showing 1 - 7 results of 7 for search 'Lina Ghaloul-Gonzalez', query time: 0.03s Refine Results
  1. 1
    A familial case of mutation with variable expressivity

    A familial case of mutation with variable expressivity by Paige Heiman, Sarah Drewes, Lina Ghaloul-Gonzalez

    Published 2021-02-01
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  2. 2
    Medium chain acyl-CoA dehydrogenase deficiency in a premature infant

    Medium chain acyl-CoA dehydrogenase deficiency in a premature infant by Steven F. Dobrowolski, Lina Ghaloul-Gonzalez, Jerry Vockley

    Published 2017-11-01
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  3. 3
    Natural history of propionic acidemia in the Amish population

    Natural history of propionic acidemia in the Amish population by Sarah Ehrenberg, Catherine Walsh Vockley, Paige Heiman, Zineb Ammous, Olivia Wenger, Jerry Vockley, Lina Ghaloul-Gonzalez

    Published 2022-12-01
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  4. 4
    Identification of Two Homozygous Variants in <i>MYBPC3</i> and <i>SMYD1</i> Genes Associated with Severe Infantile Cardiomyopathy

    Identification of Two Homozygous Variants in <i>MYBPC3</i> and <i>SMYD1</i> Genes Associated with Severe Infantile Cardiomyopathy by Marta W. Szulik, Miguel Reyes-Múgica, Daniel F. Marker, Ana M. Gomez, Matthew D. Zinn, Leslie K. Walsh, Juan Pablo Ochoa, Sarah Franklin, Lina Ghaloul-Gonzalez

    Published 2023-03-01
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  5. 5
    P257: A single institution analysis of in-house whole genome sequencing within pediatric and neonatal intensive care units (The PISCES Study)

    P257: A single institution analysis of in-house whole genome sequencing within pediatric and neonatal intensive care units (The PISCES Study) by Peter Nelson, Cate Walsh Vockley, Georgianne Arnold, Jirair Bedoyan, Amina Kunovac, Lindsey Kelly, Dara Kozak, Alexander Yatsenko, Jennifer Atkinson, Adrian Lee, Daniel Bellissimo, Jerry Vockley, Lina Ghaloul-Gonzalez

    Published 2023-01-01
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  6. 6
    ITCH deficiency clinical phenotype expansion and mitochondrial dysfunction

    ITCH deficiency clinical phenotype expansion and mitochondrial dysfunction by Rachel Wolfe, Paige Heiman, Olivia D'Annibale, Anuradha Karunanidhi, Alyssa Powers, Marianne Mcguire, Bianca Seminotti, Steven F. Dobrowolski, Miguel Reyes-Múgica, Kathryn S. Torok, Al-Walid Mohsen, Jerry Vockley, Lina Ghaloul-Gonzalez

    Published 2022-12-01
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  7. 7
    A porcine model of phenylketonuria generated by CRISPR/Cas9 genome editing

    A porcine model of phenylketonuria generated by CRISPR/Cas9 genome editing by Erik A. Koppes, Bethany K. Redel, Marie A. Johnson, Kristen J. Skvorak, Lina Ghaloul-Gonzalez, Megan E. Yates, Dale W. Lewis, Susanne M. Gollin, Yijen L. Wu, Shawn E. Christ, Martine Yerle, Angela Leshinski, Lee D. Spate, Joshua A. Benne, Stephanie L. Murphy, Melissa S. Samuel, Eric M. Walters, Sarah A. Hansen, Kevin D. Wells, Uta Lichter-Konecki, Robert A. Wagner, Joseph T. Newsome, Steven F. Dobrowolski, Jerry Vockley, Randall S. Prather, Robert D. Nicholls

    Published 2020-10-01
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