Search Results - Joel B. Krier

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    A novel variant in the GNAS complex locus causes Albright hereditary osteodystrophy with pseudopseudohypoparathyroidism by Jeffrey S. Smith, MD, PhD, Abdulrahman A. Aldeeri, MD, Scott A. Elman, MD, Joel B. Krier, MD, Joseph F. Merola, MD, MMSc

    Published 2022
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    The BabySeq project: implementing genomic sequencing in newborns by Ingrid A. Holm, Pankaj B. Agrawal, Ozge Ceyhan-Birsoy, Kurt D. Christensen, Shawn Fayer, Leslie A. Frankel, Casie A. Genetti, Joel B. Krier, Rebecca C. LaMay, Harvey L. Levy, Amy L. McGuire, Richard B. Parad, Peter J. Park, Stacey Pereira, Heidi L. Rehm, Talia S. Schwartz, Susan E. Waisbren, Timothy W. Yu, The BabySeq Project Team, Robert C. Green, Alan H. Beggs

    Published 2018
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