Uterine cancer in Jewish Israeli BRCA1/2 mutation carriers by Laitman, Yael, Michaelson‐Cohen, Rachel, Levi, Einat, Chen‐Shtoyerman, Rakefet, Reish, Orit, Josefsberg Ben‐Yehoshua, Sagi, Bernstein‐Molho, Rinat, Keinan‐Boker, Lital, Rosengarten, Ora, Silverman, Barbara G., Perri, Tamar, Korach, Jacob, Mor, Pnina, Ephrat Ben‐Baruch, Noa, Levy Lahad, Ephrat, Friedman, Eitan

Get full text

MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome by Zung, Amnon, Petek, Erwin, Ben‐Zeev, Bruria, Schwarzbraun, Thomas, Ben‐Yehoshua, Sagi Josefsberg

Get full text

Fetal exome sequencing: yield and limitations in a tertiary referral center by Daum, H., Meiner, V., Elpeleg, O., Harel, T., Bar‐Or, Libat, Eilat, Avital, Fahham, Duha, Gur, Michal, Hacohen, Nuphar, Kimchi, Adva, Macarov, Michal, Porat, Shay, Rosenak, Daniel, Shaag, Avraham, Shkedi‐Rafid, Shiri, Szmulewicz, Adi, Yagel, Simcha, Yanai, Nili, Zvi, Naama, Banne, Ehud, Ben‐Yehoshua, Sagi Josefsberg, Ephron, Noa, Lev, Dorit, Drugan, Arie, Irge, Dana, Mordechai, Shikma, Yehuda, Adi Ben, Freireich, Orit, Segel, Reeval

Get full text

The rare 13q33–q34 microdeletions: eight new patients and review of the literature by Sagi-Dain, Lena, Goldberg, Yael, Peleg, Amir, Sukenik-Halevy, Rivka, Sofrin-Drucker, Efrat, Appelman, Zvi, Josefsberg, Ben Yehoshua Sagi, Ben-Shachar, Shay, Vinkler, Chana, Basel-Salmon, Lina, Maya, Idit

Get full text

The phenotype of 15 cases with rare 8q24.13‐q24.3 deletions–A new syndrome or still an enigma? by Maya, Idit, Kahana, Sarit, Agmon‐Fishman, Ifaat, Klein, Cochava, Matar, Reut, Berger, Racheli, Josefsberg, Sagi Ben Yehoshua, Shohat, Mordechai, Marom, Daphna, Basel‐Salmon, Lina, Sagi‐Dain, Lena

Get full text

Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study by Bancroft, Elizabeth K, Page, Elizabeth C, Castro, Elena, Lilja, Hans, Vickers, Andrew, Sjoberg, Daniel, Assel, Melissa, Foster, Christopher S, Drew, Kate, Mæhle, Lovise, Axcrona, Karol, Evans, D. Gareth, Bulman, Barbara, Eccles, Diana, van Asperen, Christi, Vasen, Hans, Kiemeney, Lambertus A, Ringelberg, Janneke, Cybulski, Cezary, Wokolorczyk, Dominika, Selkirk, Christina, Hulick, Peter J, Bojesen, Anders, Skytte, Anne-Bine, Lam, Jimmy, Taylor, Louise, Oldenburg, Rogier, Verhaegh, Gerald, van Zelst-Stams, Wendy A, Oosterwijk, Jan C, Blanco, Ignacio, Salinas, Monica, Cook, Jackie, Rosario, Derek J, Buys, Saundra, Conner, Tom, Ausems, Margreet G, Ong, Kai-ren, Hoffman, Jonathan, Domchek, Susan, Teixeira, Manuel R, Maia, Sofia, Foulkes, William D, Taherian, Nassim, Ruijs, Marielle, den Enden, Apollonia T. Helderman-van, Izatt, Louise, Davidson, Rosemarie, Adank, Muriel A, Walker, Lisa, Schmutzler, Rita, Tucker, Kathy, Kirk, Judy, Hodgson, Shirley, Harris, Marion, Douglas, Fiona, Lindeman, Geoffrey J, Zgajnar, Janez, Tischkowitz, Marc, Susman, Rachel, Ramón y Cajal, Teresa, Patcher, Nicholas, Spigelman, Allan, Liljegren, Annelie, Side, Lucy, Brewer, Carole, Donaldson, Alan, Stefansdottir, Vigdis, Chen-Shtoyerman, Rakefet, Amor, David J, Barwell, Julian, Giri, Veda N, Murthy, Vedang, Nicolai, Nicola, Teo, Soo-Hwang, Greenhalgh, Lynn, Strom, Sara, Henderson, Alex, McGrath, John, Gallagher, David, Aaronson, Neil, Ardern-Jones, Audrey, Bangma, Chris, Dearnaley, David, Eyfjord, Jorunn, Rothwell, Jeanette, Falconer, Alison, Gronberg, Henrik, Johannsson, Oskar, Kote-Jarai, Zsofia, Axcrona, Ulrika, Melia, Jane, McKinley, Joanne, Mitra, Anita V, Moynihan, Clare, Rennert, Gad, Suri, Mohnish, Wilson, Penny, Killick, Emma, Moss, Sue

Get full text

A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study by Page, Elizabeth C, Brook, Mark N, McHugh, Jana, Jones, Ann-Britt, Merson, Susan, Ong, Kai Ren, Hoffman, Jonathan, Huber, Camilla, Grindedal, Eli Marie, Stormorken, Astrid, Hanson, Helen, James, Paul, Syngal, Sapna, Barwell, Julian, Teixeira, Manuel R, Macrae, Finlay A, Pachter, Nicholas, Buys, Saundra, Cooney, Kathleen A, Taylor, Amy, Hogben, Matthew, Castro, Elena, Dearnaley, David, Dias, Alexander, Dudderidge, Tim, Hamdy, Freddie C, Mikropoulos, Christos, Mitra, Anita V, Moynihan, Clare, Rennert, Gad, Collier, Rebecca, Adlard, Julian, Alfonso, Rosa, Ball, Darran, Benton, Barbara, Biller, Leah, Burgess, Lucy, Callard, Alice, Carter, Vanda, Catanzaro, Mario, Compton, Cecilia, Cornford, Philip, Costello, Philandra, Coulier, Laura, Douglas, Fiona, Douglas, Emma, Ellery, Natalie, Frydenberg, Mark, Fuller, Debbie, Gabriel, Camila, Genova, Elena, George, Angela, Georgiou, Demetra, Goff, Sally, Goldgar, David, Goodman, Selina, Gray, Catherine, Griffiths, Julie, Gupwell, Karin, Hart, Rachel, Hawkes, Lara, Hilario, Kathrine, Hulick, Peter, Jenkins, Sharon, Josefsberg Ben-Yehoshua, Sagi, Kinsella, Netty, Kumar, Pardeep, Leibovici, Dan, Martin, Phoebe, Murphy, Morgan, Mzazi, Shumi, Nadolski, Maria, Park, Linda, Patel, Nafisa, Paulo Souto, João, Peixoto, Ana, Petelin, Lara, Poile, Charlotte, Purnell, Helen, Rankin, Brigette, Renton, Caroline, Sajoo, Anaar, Saunders, Kathryn, Searle, Anne, Sehra, Ravinder, Shackleton, Kylie, Shaw, Adam, Shevrin, Daniel, Siguake, Kas, Snadden, Lesley, Sorrentino, Margherita, Thomas, Maggie, Townshend, Sharron, Tricker, Karen, Tripathi, Vishakha, Valdagni, Riccardo, Verdon, Lizzie, Vogel, Kristen, Watford, Amy, Offman, Judith

Get full text

Is fetal isolated double renal collecting system an indication for chromosomal microarray? by Singer, Amihood, Maya, Idit, Frumkin, Ayala, Zeligson, Sharon, Josefsberg, Sagi Ben Yehoshua, Berger, Racheli, Shachar, Shay Ben, Sagi-Dain, Lena

Get full text

MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome by Zung, Amnon, Petek, Erwin, Ben-Zeev, Bruria, Schwarzbraun, Thomas, Ben-Yehoshua, Sagi Josefsberg

Get full text