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Open Access

Peer-reviewed

Research Article

Unique Alterations of an Ultraconserved Non-Coding Element in the 3′UTR of ZIC2 in Holoprosencephaly

  • Erich Roessler,

    Affiliation Medical Genetics Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Ping Hu,

    Affiliation Medical Genetics Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Sung-Kook Hong,

    Affiliation Medical Genetics Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Kshitij Srivastava,

    Affiliation Medical Genetics Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Blake Carrington,

    Affiliation Zebrafish Core Facility, Genetics and Molecular Biology Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Raman Sood,

    Affiliation Zebrafish Core Facility, Genetics and Molecular Biology Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Hanna Petrykowska,

    Affiliation Genome Technology Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Laura Elnitski,

    Affiliation Genome Technology Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Lucilene A. Ribeiro,

    Affiliation Molecular Genetics Laboratory and Clinical Genetics Service, Hospital for Rehabilitation and Craniofacial Anomalies, USP, Bauru, Brazil

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  • Antonio Richieri-Costa,

    Affiliation Molecular Genetics Laboratory and Clinical Genetics Service, Hospital for Rehabilitation and Craniofacial Anomalies, USP, Bauru, Brazil

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  • Benjamin Feldman,

    Affiliation Medical Genetics Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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  • Ward F. Odenwald,

    Affiliation Neural Cell-Fate Determinants Section, National Institute of Neurological Diseases and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Maximilian Muenke

    mamuenke@mail.nih.gov

    Affiliation Medical Genetics Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, United States of America

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