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Gtf2i and Gtf2ird1 mutation are not sufficient to reproduce mouse phenotypes caused by the Williams Syndrome critical region
Nathan Kopp, Katherine McCullough, Susan E. Maloney, View ORCID ProfileJoseph D. Dougherty
doi: https://doi.org/10.1101/558544
Nathan Kopp
1Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA
2Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA
Katherine McCullough
1Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA
2Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA
Susan E. Maloney
2Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA
3Intellectual and Developmental Disabilities Research Center, Washington University School of Medicine, St. Louis, MO, USA
Joseph D. Dougherty
1Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA
2Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA
3Intellectual and Developmental Disabilities Research Center, Washington University School of Medicine, St. Louis, MO, USA
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Posted February 24, 2019.
Gtf2i and Gtf2ird1 mutation are not sufficient to reproduce mouse phenotypes caused by the Williams Syndrome critical region
Nathan Kopp, Katherine McCullough, Susan E. Maloney, Joseph D. Dougherty
bioRxiv 558544; doi: https://doi.org/10.1101/558544
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