Search Results - Lindsay Williams

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    Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism by Rebelo, Adriana P., Jeanne, Médéric, Danzi, Matt C., Tekin, Mustafa, Acosta, Maria T., Andrews, Ashley, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Butte, Manish J., Byrd, William E., Cassini, Thomas, Chao, Hsiao‐Tuan, Coakley, Terra R., Cobban, Laurel A., Cole, F. Sessions, Colley, Heather A., Corner, Brian, Dai, Hongzheng, Davis, Joie, Delgado, Margaret, Douine, Emilie D., Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Fisher, Paul G., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Horike‐Pyne, Martha, Huang, Alden, Izumi, Kosuke, Jean‐Marie, Orpa, Jobanputra, Vaidehi, Ketkar, Shamika, Kohler, Jennefer N., Kravets, Elijah, Lalani, Seema R., Latchman, Kumarie, LeBlanc, Kimberly, Lewis, Richard A., Liu, Pengfei, Loo, Sandra K., MacRae, Calum A., Maghiro, AudreyStephannie C., Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Marth, Gabor, Martínez‐Agosto, Julian A., McConkie‐Rosell, Allyn, Morava, Eva, Moretti, Paolo, Morimoto, Marie, Neumann, Serena, Novacic, Donna, Oglesbee, Devin, Papp, Jeanette C., Petcharet, Leoyklang, Posey, Jennifer E., Potocki, Lorraine, Rao, Deepak A., Raskind, Wendy, Rosenfeld, Jill A., Sabaii, Marla, Scott, Daryl A., Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Sisco, Kathy, Smith, Edward C., Smith, Carson A., Smith, Kevin S., Solomon, Ben, Stergachis, Andrew, Sullivan, Kathleen, Tabor, Holly K., Tan, Queenie K.‐G., Thorson, Willa, Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wenger, Tara, Westerfield, Monte, Worley, Kim

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    Databases for Congenital Heart Defect Public Health Studies Across the Lifespan by Riehle‐Colarusso, Tiffany J., Cassell, Cynthia H., Gray, Darryl T., Grosse, Scott D., Jacobs, Marshall L., Wood, Thalia, Oster, Matthew E., Abarbanell, Ginnie Lee, Adams, Faith, Allen, Sydney, Ambrose, Anand, Backer, Carl Lewis, Baker‐Smith, Carissa Marie, Basken, Amy, Beekman, Robert H., Bockerstette, JR, Boris, Jeffrey R., Hageman, Dana Brock, Soto, Cheryl Brosig, Campbell, Robert M., Coleman, Christina, Couser, Chris, Crenshaw, Melissa Lynnn, Crume, Tessa, Daskalov, Rachel, Del Monte, Mark D., Eghtesady, Pirooz, Feldkamp, Marcia, Foley, William, Foster, Elyse, Galioto, Frank M., Gore, Lorraine A., Gray, Johanna, Grosse, Scott D., Gurvitz, Michelle Z., Handa, Sonia, Heath, Emilie, Hile, Danielle, Hokanson, John Smith, Hubbell, Marius M., Huhn, Kelly, Kasnic, David, Kemper, Alex R., Kenny, Natalie, King, Valerie, Knapp, Donna, Kobayashi, Daisuke, Kovacs, Adrienne, Kucik, James, Kuehl, Karen S., Lemacks, Jodi, Libby, Patty, Lloyd‐Puryear, Michele Ann, Madsen, Nicolas L., Mai, Cara, Mann, Monica, Paul Matherne, G., Mauller, Phillip, May, Susan, McCabe, Edward R. B., McCabe, Nancy, McCardle, Michelle, McCormick, Kristine Brite, Mitchell, Stephanie, Morris, Laura, Mussatto, Kathleen, Nelson, Sue, Nicolarsen, Jeremy, Niggles, Autumn, Noonan, Jacqueline Anne, Ober, Gail, Patel, Mehul D., Patel, Jasmin, Pinto, Nelangi M., Polen, Kara, Rintamaki, Michelle, Rush, Grahame, Russell, Laura, Sable, Craig Andrew, Saltz, Joel, Schubert, Kathryn, Schwartz, Vida, Shapira, Stuart K., Silverman, Brenda, Smith, Juanita, Smith, Kimberly E., Smith, Kristina, Srivastava, Shubhika, Taubert, Kathryn, Thibadeau, Judy, Thomas, John P., Thomas, Dena, Timmins, Susan, Torentinos, Natalie, Tringali, Glenn, Tweddell, James S., Ware, Janice, Weiss, Marina, Whitley, Herbert, Wright, Matthew

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    Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome by Pujol‐Giménez, Jonai, Miller, Danny E., Allworth, Aimee, Chanprasert, Sirisak, Folta, Andrew B., Hing, Anne, Horike‐Pyne, Martha, Leppig, Kathleen A., Parhin, Azma, Rosenthal, Elisabeth A., Schwarze, Ulrike, Strohbehn, Samuel, Sybert, Virginia P., Timms, Andrew, Wener, Mark, Bamshad, Michael J., Bacus, Tamara J., Blue, Elizabeth E., Brower, Katherine, Sánchez, Diana Cornejo, Gomeztagle‐Burgess, Katherine, Hurless, Jameson R., Shively, Kathryn M., Weiss, Jeffrey M., Wheeler, Marsha M., Adam, Margaret, Alvey, Justin, Amendola, Laura, Andrews, Ashley, Ashley, Euan A., Barbouth, Deborah, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Bivona, Stephanie, Blue, Elizabeth, Bonner, Devon, Byers, Peter, Cassini, Thomas, Chang, Ta Chen Peter, Chanprasert, Sirisak, Clark, Gary D., Cole, F. Sessions, Corona, Rosario, Crouse, Andrew B., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Emrick, Lisa T., Fisher, Paul G., Gahl, William A., Hadley, Don, Hahn, Sihoun, High, Frances, Hing, Anne, Hisama, Fuki M., Horike‐Pyne, Martha, Hutchison, Sarah, Izumi, Kosuke, Kohane, Isaac S., Kohler, Jennefer N., Lalani, Seema R., Lam, Byron, Lanpher, Brendan C., Lewis, Richard A., Liu, Xue Zhong, Maduro, Valerie V., Manolio, Teri A., McCauley, Jacob, McCray, Alexa T., Mefford, Heather, Moretti, Paolo, Nickerson, Deborah, Nieves‐Rodriguez, Shirley, Orengo, James P., Pak, Stephen, Papp, Jeanette C., Parker, Neil H., Phillips, John A., Rao, Deepak A., Raskind, Wendy, Renteria, Genecee, Rosenfeld, Jill A., Saporta, Mario, Schaechter, Judy, Scott, Daryl A., Sisco, Kathy, Spillmann, Rebecca C., Sullivan, Jennifer A., Tabor, Holly K., Tifft, Cynthia J., Ungar, Rachel A., Walker, Melissa, Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Wener, Mark, Yamamoto, Shinya, Dipple, Katrina M., Stergachis, Andrew B.

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