Selected Papers on Calculus by Bernstein, Dorothy K.

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Reviews by Snell, J. Laurie, Lewis, James V., Casstevens, Thomas W., Berman, Elizabeth, Hageman, L. A., Bernstein, Dorothy K., Brungs, H. H., Divinsky, N.

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability by Küry, Sébastien, van Woerden, Geeske M., Besnard, Thomas, Proietti Onori, Martina, Latypova, Xénia, Towne, Meghan C., Cho, Megan T., Ploeg, Melissa A., Sanders, Stephan, Stessman, Holly A.F., Pujol, Aurora, Distel, Ben, Robak, Laurie A., Bernstein, Jonathan A., Denommé-Pichon, Anne-Sophie, Lesca, Gaëtan, Sellars, Elizabeth A., Berg, Jonathan, Carré, Wilfrid, Busk, Øyvind Løvold, van Bon, Bregje W.M., Waugh, Jeff L., Deardorff, Matthew, Hoganson, George E., Bosanko, Katherine B., Johnson, Diana S., Dabir, Tabib, Holla, Øystein Lunde, Sarkar, Ajoy, Tveten, Kristian, de Bellescize, Julitta, Braathen, Geir J., Terhal, Paulien A., Grange, Dorothy K., van Haeringen, Arie, Lam, Christina, Mirzaa, Ghayda, Burton, Jennifer, Bhoj, Elizabeth J., Douglas, Jessica, Santani, Avni B., Nesbitt, Addie I., Helbig, Katherine L., Andrews, Marisa V., Begtrup, Amber, Tang, Sha, van Gassen, Koen L.I., Juusola, Jane, Foss, Kimberly, Enns, Gregory M., Moog, Ute, Hinderhofer, Katrin, Paramasivam, Nagarajan, Lincoln, Sharyn, Kusako, Brandon H., Lindenbaum, Pierre, Charpentier, Eric, Nowak, Catherine B., Cherot, Elouan, Simonet, Thomas, Ruivenkamp, Claudia A.L., Hahn, Sihoun, Brownstein, Catherine A., Xia, Fan, Schmitt, Sébastien, Deb, Wallid, Bonneau, Dominique, Nizon, Mathilde, Chelly, Jamel, Rudolf, Gabrielle, Sanlaville, Damien, Parent, Philippe, Gilbert-Dussardier, Brigitte, Toutain, Annick, Sutton, Vernon R., Thies, Jenny, Peart-Vissers, Lisenka E.L.M., Boisseau, Pierre, Vincent, Marie, Grabrucker, Andreas M., Dubourg, Christèle, Tan, Wen-Hann, Verbeek, Nienke E., Granzow, Martin, Santen, Gijs W.E., Shendure, Jay, Pasquier, Laurent, Redon, Richard, Yang, Yaping, State, Matthew W., Kleefstra, Tjitske, Cogné, Benjamin, Petrovski, Slavé, Retterer, Kyle, Eichler, Evan E., Rosenfeld, Jill A., Agrawal, Pankaj B., Bézieau, Stéphane, Odent, Sylvie, Mercier, Sandra

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Moving AHEAD with an international human epigenome project by Jones, PA, Archer, TK, Baylin, SB, Beck, S, Berger, S, Bernstein, BE, Carpten, JD, Clark, SJ, Costello, JF, Doerge, RW, Esteller, M, Feinberg, AP, Gingeras, TR, Greally, JM, Henikoff, S, Herman, JG, Jackson-Grusby, L, Jenuwein, T, Jirtle, RL, Kim, YJ, Laird, PW, Lim, B, Martienssen, R, Polyak, K, Stunnenberg, H, Tlsty, TD, Tycko, B, Ushijima, T, Zhu, JD, Pirrotta, V, Allis, CD, Elgin, SC, Rine, J, Wu, C

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Clinical and radiographic delineation of Bent Bone Dysplasia-FGFR2 type or Bent Bone Dysplasia with Distinctive Clavicles and Angel-shaped Phalanges by Krakow, Deborah, Cohn, Daniel H., Wilcox, William R., Noh, Grace J., Raffel, Leslie J., Sarukhanov, Anna, Ivanova, Margarita H., Danielpour, Moise, Grange, Dorothy K., Elliott, Alison M., Bernstein, Jonathan A., Rimoin, David L., Merrill, Amy E., Lachman, Ralph S.

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Venous thromboembolic complications (VTE) in children: first analyses of the Canadian Registry of VTE by Andrew, M, David, M, Adams, M, Ali, K, Anderson, R, Barnard, D, Bernstein, M, Brisson, L, Cairney, B, DeSai, D

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