Merkel cell carcinoma : Review of 22 cases with surgical, pathologic, and therapeutic considerations by GOLLARD, R, WEBER, R, KOSTY, M. P, GREENWAY, H. T, MASSULLO, V, HUMBERSON, C

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Role of CAMK2D in neurodevelopment and associated conditions by Rigter, Pomme M.F., de Konink, Charlotte, Dunn, Matthew J., Proietti Onori, Martina, Humberson, Jennifer B., Thomas, Matthew, Barnes, Caitlin, Prada, Carlos E., Weaver, K. Nicole, Ryan, Thomas D., Caluseriu, Oana, Conway, Jennifer, Calamaro, Emily, Fong, Chin-To, Wuyts, Wim, Meuwissen, Marije, Hordijk, Eva, Jonkers, Carsten N., Anderson, Lucas, Yuseinova, Berfin, Polonia, Sarah, Beysen, Diane, Stark, Zornitza, Savva, Elena, Poulton, Cathryn, McKenzie, Fiona, Bhoj, Elizabeth, Bupp, Caleb P., Bézieau, Stéphane, Mercier, Sandra, Blevins, Amy, Wentzensen, Ingrid M., Xia, Fan, Rosenfeld, Jill A., Hsieh, Tzung-Chien, Krawitz, Peter M., Elbracht, Miriam, Veenma, Danielle C.M., Schulman, Howard, Stratton, Margaret M., Küry, Sébastien, van Woerden, Geeske M.

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Gain-of-function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome by Lin, Angela E., Michot, Caroline, Cormier-Daire, Valerie, L'Ecuyer, Thomas J., Matherne, G. Paul, Barnes, Barrett H., Humberson, Jennifer B., Edmondson, Andrew C., Zackai, Elaine, O'Connor, Matthew J., Kaplan, Julie D., Ebeid, Makram R., Krier, Joel, Krieg, Elizabeth, Ghoshhajra, Brian, Lindsay, Mark E.

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Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants by Jacobs, Eva Z., Brown, Kathleen, Byler, Melissa C., D'haenens, Erika, Dheedene, Annelies, Henderson, Lindsay B., Humberson, Jennifer B., Jaarsveld, Richard H., Kanani, Farah, Lebel, Robert Roger, Millan, Francisca, Oegema, Renske, Oostra, Ann, Parker, Michael J., Rhodes, Lindsay, Saenz, Margarita, Seaver, Laurie H., Si, Yue, Vanlander, Arnaud, Vergult, Sarah, Callewaert, Bert

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NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain by Liu, Sanxiong, Aldinger, Kimberly A., Cheng, Chi Vicky, Kiyama, Takae, Dave, Mitali, McNamara, Hanna K., Zhao, Wukui, Stafford, James M., Descostes, Nicolas, Lee, Pedro, Caraffi, Stefano G., Ivanovski, Ivan, Errichiello, Edoardo, Zweier, Christiane, Zuffardi, Orsetta, Schneider, Michael, Papavasiliou, Antigone S., Perry, M. Scott, Humberson, Jennifer, Cho, Megan T., Weber, Astrid, Swale, Andrew, Badea, Tudor C., Mao, Chai-An, Garavelli, Livia, Dobyns, William B., Reinberg, Danny

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NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain by Liu, Sanxiong, Aldinger, Kimberly A., Cheng, Chi Vicky, Kiyama, Takae, Dave, Mitali, McNamara, Hanna K., Zhao, Wukui, Stafford, James M., Descostes, Nicolas, Lee, Pedro, Caraffi, Stefano G., Ivanovski, Ivan, Errichiello, Edoardo, Zweier, Christiane, Zuffardi, Orsetta, Schneider, Michael, Papavasiliou, Antigone S., Perry, M. Scott, Humberson, Jennifer, Cho, Megan T., Weber, Astrid, Swale, Andrew, Badea, Tudor C., Mao, Chai-An, Garavelli, Livia, Dobyns, William B., Reinberg, Danny

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Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability by Cogné, Benjamin, Ehresmann, Sophie, Beauregard-Lacroix, Eliane, Rousseau, Justine, Besnard, Thomas, Garcia, Thomas, Petrovski, Slavé, Avni, Shiri, McWalter, Kirsty, Blackburn, Patrick R., Sanders, Stephan J., Uguen, Kévin, Harris, Jacqueline, Cohen, Julie S., Blyth, Moira, Lehman, Anna, Berg, Jonathan, Li, Mindy H., Kini, Usha, Joss, Shelagh, von der Lippe, Charlotte, Gordon, Christopher T., Sutton, Vernon R., Johnston, Jennifer J., Poduri, Annapurna, Nordenskjöld, Magnus, Shashi, Vandana, Gerkes, Erica H., Bongers, Ernie M.H.F., Gilissen, Christian, Zarate, Yuri A., Kvarnung, Malin, Lally, Kevin P., Kulch, Peggy A., Daniels, Brina, Hernandez-Garcia, Andres, Stong, Nicholas, Retterer, Kyle, Sullivan, Jennifer, Geisheker, Madeleine R., Stray-Pedersen, Asbjorg, Tarpinian, Jennifer M., Sapp, Julie C., Zyskind, Jacob, Holla, Øystein L., Bedoukian, Emma, Filippini, Francesca, Guimier, Anne, Picard, Arnaud, Busk, Øyvind L., Punetha, Jaya, Pfundt, Rolph, Lindstrand, Anna, Nordgren, Ann, Kalb, Fayth, Desai, Megha, Ebanks, Ashley Harmon, Jhangiani, Shalini N., Zackai, Elaine H., Begtrup, Amber, Song, Xiaofei, Toutain, Annick, Wentzensen, Ingrid M., Odent, Sylvie, Bonneau, Dominique, Latypova, Xénia, Deb, Wallid, Redon, Sylvia, Bilan, Frédéric, Legendre, Marine, Troyer, Caitlin, Whitlock, Kerri, Caluseriu, Oana, Pichurin, Pavel N., Gavrilova, Ralitza, Rinne, Tuula, Park, Meredith, Shain, Catherine, Heinzen, Erin L., Xiao, Rui, Amiel, Jeanne, Isidor, Bertrand, Biesecker, Leslie G., Lowenstein, Dan, Posey, Jennifer E., Denommé-Pichon, Anne-Sophie, Férec, Claude, Yang, Xiang-Jiao, Rosenfeld, Jill A., Gilbert-Dussardier, Brigitte, Audebert-Bellanger, Séverine, Stessman, Holly A.F., Nellaker, Christoffer, Yang, Yaping, Lupski, James R., Eichler, Evan E., Bolduc, Francois, Bézieau, Stéphane, Küry, Sébastien, Campeau, Philippe M.

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