Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5 by McMillin, Margaret J., Beck, Anita E., Chong, Jessica X., Shively, Kathryn M., Buckingham, Kati J., Gildersleeve, Heidi I.S., Aracena, Mariana I., Aylsworth, Arthur S., Bitoun, Pierre, Carey, John C., Clericuzio, Carol L., Crow, Yanick J., Curry, Cynthia J., Devriendt, Koenraad, Everman, David B., Fryer, Alan, Gibson, Kate, Giovannucci Uzielli, Maria Luisa, Graham, John M., Hall, Judith G., Hecht, Jacqueline T., Heidenreich, Randall A., Hurst, Jane A., Irani, Sarosh, Krapels, Ingrid P.C., Leroy, Jules G., Mowat, David, Plant, Gordon T., Robertson, Stephen P., Schorry, Elizabeth K., Scott, Richard H., Seaver, Laurie H., Sherr, Elliott, Splitt, Miranda, Stewart, Helen, Stumpel, Constance, Temel, Sehime G., Weaver, David D., Whiteford, Margo, Williams, Marc S., Tabor, Holly K., Smith, Joshua D., Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J.

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Genotype-phenotype relationships in Freeman-Sheldon syndrome by Beck, Anita E., McMillin, Margaret J., Gildersleeve, Heidi I. S., Shively, Kathryn M. B., Tang, Andy, Bamshad, Michael J.

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Spectrum of mutations that cause distal arthrogryposis types 1 and 2B by Beck, Anita E., McMillin, Margaret J., Gildersleeve, Heidi I.S., Kezele, Phillip R., Shively, Kathryn M., Carey, John C., Regnier, Michael, Bamshad, Michael J.

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HyCCAPP as a tool to characterize promoter DNA-protein interactions in Saccharomyces cerevisiae by Guillen-Ahlers, Hector, Rao, Prahlad K., Levenstein, Mark E., Kennedy-Darling, Julia, Perumalla, Danu S., Jadhav, Avinash Y.L., Glenn, Jeremy P., Ludwig-Kubinski, Amy, Drigalenko, Eugene, Montoya, Maria J., Göring, Harald H., Anderson, Corianna D., Scalf, Mark, Gildersleeve, Heidi I.S., Cole, Regina, Greene, Alexandra M., Oduro, Akua K., Lazarova, Katarina, Cesnik, Anthony J., Barfknecht, Jared, Cirillo, Lisa A., Gasch, Audrey P., Shortreed, Michael R., Smith, Lloyd M., Olivier, Michael

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