Cardiotoxicity screening of long‐term, breast cancer survivors—The CAROLE (Cardiac‐Related Oncologic Late Effects) Study von Puckett, Lindsay L., Saba, Shahryar G., Henry, Sonia, Rosen, Stacey, Rooney, Elise, Filosa, Samaria L., Gilbo, Philip, Pappas, Karalyn, Laxer, Alison, Eacobacci, Katherine, Kapyur, Amitha N., Robeny, Justin, Musial, Samantha, Chaudhry, Anisha, Chaudhry, Rahul, Lesser, Martin L., Riegel, Adam, Ramoutarpersaud, Sariah, Rahmani, Navid, Shah, Amar, Papas, Vivian, Dawodu, Toluwani, Charlton, Jessica, Knisely, Jonathan P. S., Lee, Lucille

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The CAROLE (CArdiac Related Oncologic Late Effects) Study: A Phase II, single-arm feasibility trial von Puckett, Lindsay, Saba, Shahryar, Henry, Sonia, Rosen, Stacey, Rooney, Elise, Laxer, Alison, Gilbo, Philip, Pappas, Karalyn, Eacobacci, Katherine, Kapyur, Amitha, Robeny, Justin, Filosa, Samaria, Musial, Samantha, Chaudhry, Anisha, Chaudhry, Rahul, Lesser, Martin, Riegel, Adam, Charlton, Jessica, Ramoutarpersaud, Sariah, Lee, Lucille

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Classification Criteria for Axial Disease in Youth With Juvenile Spondyloarthritis von Weiss, Pamela F., Brandon, Timothy G., Aggarwal, Amita, Burgos‐Vargas, Ruben, Colbert, Robert A., Horneff, Gerd, Laxer, Ronald M., Minden, Kirsten, Ravelli, Angelo, Ruperto, Nicolino, Smith, Judith A., Stoll, Matthew L., Tse, Shirley M., Van den Bosch, Filip, Maksymowych, Walter P., Lambert, Robert G., Biko, David M., Chauvin, Nancy A., Francavilla, Michael L., Jaremko, Jacob L., Herregods, Nele, Kasapcopur, Ozgur, Yildiz, Mehmet, Srinivasalu, Hemalatha, Lovell, Daniel J., Nigrovic, Peter A., Foeldvari, Ivan, Klein‐Gitelman, Marisa S., Ozen, Seza, Naden, Ray, Hendry, Alison M., Joos, Rik

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Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD) von Chakraborty, Pranesh K., Schmitz-Abe, Klaus, Kennedy, Erin K., Mamady, Hapsatou, Naas, Turaya, Durie, Danielle, Campagna, Dean R., Lau, Ashley, Sendamarai, Anoop K., Wiseman, Daniel H., May, Alison, Jolles, Stephen, Connor, Philip, Powell, Colin, Heeney, Matthew M., Giardina, Patricia-Jane, Klaassen, Robert J., Kannengiesser, Caroline, Thuret, Isabelle, Thompson, Alexis A., Marques, Laura, Hughes, Stephen, Bonney, Denise K., Bottomley, Sylvia S., Wynn, Robert F., Laxer, Ronald M., Minniti, Caterina P., Moppett, John, Bordon, Victoria, Geraghty, Michael, Joyce, Paul B.M., Markianos, Kyriacos, Rudner, Adam D., Holcik, Martin, Fleming, Mark D.

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SARS-CoV-2 infection in technology-dependent children: a multicenter case series von Robinson, Joan, Dewan, Tammie, Morris, Shaun K., Bitnun, Ari, Gill, Peter, Tal, Tala El, Laxer, Ronald M., Yeh, E. Ann, Yea, Carmen, Ulloa-Gutierrez, Rolando, Brenes-Chacon, Helena, Yock-Corrales, Adriana, Ivankovich-Escoto, Gabriela, Soriano-Fallas, Alejandra, Mezerville, Marcela Hernandez-de, Papenburg, Jesse, Lefebvre, Marie-Astrid, Nateghian, Alireza, Aski, Behzad Haghighi, Manafi, Ali, Dwilow, Rachel, Bullard, Jared, Cooke, Suzette, Restivo, Lea, Lopez, Alison, Sadarangani, Manish, Roberts, Ashley, Le Saux, Nicole, Bowes, Jennifer, Purewal, Rupeena, Lautermilch, Janell, Wong, Jacqueline K., Piche, Dominique, Top, Karina A., Foo, Cheryl, Panetta, Luc, Merckx, Joanna, Barton, Michelle

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Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa von Davidson, Alice E., Schwarz, Nele, Zelinger, Lina, Stern-Schneider, Gabriele, Shoemark, Amelia, Spitzbarth, Benjamin, Gross, Menachem, Laxer, Uri, Sosna, Jacob, Sergouniotis, Panagiotis I., Waseem, Naushin H., Wilson, Robert, Kahn, Richard A., Plagnol, Vincent, Wolfrum, Uwe, Banin, Eyal, Hardcastle, Alison J., Cheetham, Michael E., Sharon, Dror, Webster, Andrew R.

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Two amino acid substitutions in apolipoprotein B are in complete allelic association with the antigen group (x/y) polymorphism : evidence for little recombination in the 3' end of... von DUNNING, A. M, RENGES, H.-H, ROSSENEU, M, TALMUD, P, HUMPHRIES, S. E, CHUN-FANG XU, PEACOCK, R, BRASSEUR, R, LAXER, G, TIKKANEN, M. J, BÜTLER, R, SAHA, N, HAMSTEN, A

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