Search Results - LaFond, Rebecca B

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    De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects by Calabretta, Sara, Boudrahem-Addour, Nassima, Joset, Pascal, Krier, Joel, Adams, David R., Allard, Patrick, Azamian, Mahshid S., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bejerano, Gill, Bellen, Hugo J., Bernstein, Jonathan A., Bick, David P., Bonner, Devon, Boone, Braden E., Brush, Matthew, Burke, Elizabeth A., Burrage, Lindsay C., Carrasquillo, Olveen, Coakley, Terra R., Cobban, Laurel A., Colley, Heather A., Cooper, Cynthia M., D’Souza, Precilla, Davids, Mariska, Dell’Angelica, Esteban C., Dhar, Shweta U., Dorset, Daniel C., Duncan, Laura, Emrick, Lisa T., Eng, Christine M., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Fieg, Elizabeth L., Gourdine, Jean-Philippe F., Grajewski, Alana, Groden, Catherine A., Gropman, Andrea L., High, Frances, Hom, Jason, Huang, Alden, Isasi, Rosario, Kelley, Emily G., Lalani, Seema R., Lanza, Ian R., Lazar, Jozef, LeBlanc, Kimberly, Lee, Hane, Levitt, Roy, Lincoln, Sharyn A., Loo, Sandra K., Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Manolio, Teri A., McCauley, Jacob, McConkie-Rosell, Allyn, McCormack, Colleen E., Morimoto, Marie, Nelson, Stan F., Newberry, J. Scott, Nicholas, Sarah K., Pallais, J. Carl, Phillips, John A., Quinlan, Aaron, Raja, Archana N., Renteria, Genecee, Robertson, Amy K., Sacco, Ralph, Scott, Daryl A., Sharma, Prashant, Shashi, Vandana, Shields, Kathleen, Shin, Jimann, Signer, Rebecca, Silverman, Edwin K., Sinsheimer, Janet S., Smith, Kevin S., Solnica-Krezel, Lilianna, Tamburro, Cecelia P., Tekin, Mustafa, Tifft, Cynthia J., Toro, Camilo, Urv, Tiina K., Velinder, Matt, Walley, Nicole M., Wangler, Michael F., Waters, Katrina M., Wegner, Daniel, Wheeler, Matthew T., Yoon, Amanda J., Yu, Guoyun, Simpson, Brittany N., Trimouille, Aurélien, Delphine, Heron, Keren, Boris, Charron, Frédéric

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