Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin von Seo, Aaron, Ben-Harosh, Miri, Sirin, Mehtap, Stein, Jerry, Dgany, Orly, Kaplelushnik, Joseph, Hoenig, Manfred, Pannicke, Ulrich, Lorenz, Myriam, Schwarz, Klaus, Stockklausner, Clemens, Walsh, Tom, Gulsuner, Suleyman, Lee, Ming K., Sendamarai, Anoop, Sanchez-Bonilla, Marilyn, King, Mary-Claire, Cario, Holger, Kulozik, Andreas E., Debatin, Klaus-Michael, Schulz, Ansgar, Tamary, Hannah, Shimamura, Akiko

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Erratum to : Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population von Steinberg-Shemer, Orna, Goldberg, Tracie A, Yacobovich, Joanne, Levin, Carina, Koren, Ariel, Revel-Vilk, Shoshana, Ben-Ami, Tal, Kuperman, Amir A, Zemer, Vered Shkalim, Toren, Amos, Kapelushnik, Joseph, Ben-Barak, Ayelet, Miskin, Hagit, Krasnov, Tanya, Noy-Lotan, Sharon, Dgany, Orly, Tamary, Hannah

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Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population von Steinberg-Shemer, Orna, Goldberg, Tracie A, Yacobovich, Joanne, Levin, Carina, Koren, Ariel, Revel-Vilk, Shoshana, Ben-Ami, Tal, Kuperman, Amir A, Zemer, Vered Shkalim, Toren, Amos, Kapelushnik, Joseph, Ben-Barak, Ayelet, Miskin, Hagit, Krasnov, Tanya, Noy-Lotan, Sharon, Dgany, Orly, Tamary, Hannah

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Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children von Gilad, Oded, Dgany, Orly, Noy-Lotan, Sharon, Krasnov, Tanya, Yacobovich, Joanne, Rabinowicz, Ron, Goldberg, Tracie, Kuperman, Amir A, Abu-Quider, Abed, Miskin, Hagit, Kapelushnik, Noa, Mandel-Shorer, Noa, Shimony, Shai, Harlev, Dan, Ben-Ami, Tal, Adam, Etai, Levin, Carina, Aviner, Shraga, Elhasid, Ronit, Berger-Achituv, Sivan, Chaitman-Yerushalmi, Lilach, Kodman, Yona, Oniashvilli, Nino, Hameiri-Grosman, Michal, Izraeli, Shai, Tamary, Hannah, Steinberg-Shemer, Orna

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Cdan1 Is Essential for Primitive Erythropoiesis von Noy-Lotan, Sharon, Dgany, Orly, Marcoux, Nathaly, Atkins, Ayelet, Kupfer, Gary M., Bosques, Linette, Gottschalk, Christine, Steinberg-Shemer, Orna, Motro, Benny, Tamary, Hannah

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Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry von TAMARY, Hannah, NISHRI, Daniella, KAPLINSKY, Chaim, BEN BARAK, Ayelet, ELHASID, Ronit, KAPELUSNIK, Joseph, KOREN, Ariel, LEVIN, Carina, ATTIAS, Dina, LAOR, Ruth, YANIV, Isaac, ROSENBERG, Philip S, YACOBOVICH, Joanne, ALTER, Blanche P, ZILBER, Rama, DGANY, Orly, KRASNOV, Tanya, AVINER, Shraga, STEPENSKY, Polina, RAVEL-VILK, Shoshana, BITAN, Menachem

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CATSPER2, a human autosomal nonsyndromic male infertility gene von Avidan, Nili, Tamary, Hannah, Dgany, Orly, Cattan, Daniel, Pariente, Alexandre, Thulliez, Michel, Borot, Nicolas, Moati, Lucien, Barthelme, Alain, Shalmon, Lea, Krasnov, Tatyana, Ben-Asher, Edna, Olender, Tsvyia, Khen, Miriam, Yaniv, Issac, Zaizov, Rina, Shalev, Hanna, Delaunay, Jean, Fellous, Marc, Lancet, Doron, Beckmann, Jacques S

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Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1 von Dgany, Orly, Avidan, Nili, Delaunay, Jean, Krasnov, Tatyana, Shalmon, Lea, Shalev, Hanna, Eidelitz-Markus, Tal, Kapelushnik, Joseph, Cattan, Daniel, Pariente, Alexandre, Tulliez, Michel, Crétien, Aurore, Schischmanoff, Pierre-Olivier, Iolascon, Achille, Fibach, Eithan, Koren, Ariel, Rössler, Jochen, Le Merrer, Martine, Yaniv, Isaac, Zaizov, Rina, Ben-Asher, Edna, Olender, Tsvyia, Lancet, Doron, Beckmann, Jacques S., Tamary, Hannah

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Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated von Noy-Lotan, Sharon, Dgany, Orly, Lahmi, Roxane, Marcoux, Nathaly, Krasnov, Tanya, Yissachar, Nissan, Ginsberg, Doron, Motro, Benny, Resnitzky, Peretz, Yaniv, Isaac, Kupfer, Gary M, Tamary, Hannah

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Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE) von Seo, Aaron, Gulsuner, Suleyman, Pierce, Sarah, Ben-Harosh, Miri, Shalev, Hanna, Walsh, Tom, Krasnov, Tanya, Dgany, Orly, Doulatov, Sergei, Tamary, Hannah, Shimamura, Akiko, King, Mary-Claire

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A Variable Clinical Presentation of Hemoglobin City of Hope von Brik Simon, Dafna, Filon, Dvora, Meiner, Vardiella, Krasnov, Tanya, Noy-Lotan, Sharon, Dgany, Orly, Gilad, Oded, Goldberg, Tracie, Izraeli, Shai, Yacobovich, Joanne, Tamary, Hannah, Steinberg-Shemer, Orna

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Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC‐Associated Neutropenia von Oz‐Alcalay, Lital, Steinberg‐Shemer, Orna, Elron, Eyal, Dvori, Michal, Elitzur, Sarah, Dgany, Orly, Noy‐Lotan, Sharon, Krasnov, Tanya, Tamary, Hannah, Brik‐Simon, Dafna, Yacobovich, Joanne, Gilad, Oded

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Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias von Noy‐Lotan, Sharon, Krasnov, Tanya, Dgany, Orly, Jeison, Marta, Yanir, Asaf D., Gilad, Oded, Toledano, Helen, Barzilai‐Birenboim, Shlomit, Yacobovich, Joanne, Izraeli, Shai, Tamary, Hannah, Steinberg‐Shemer, Orna

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Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis von Resnitzky, Peretz, Shaft, Dina, Shalev, Hanna, Kapelushnik, Joseph, Dgany, Orly, Krasnov, Tanya, Tamary, Hannah

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Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2 von Steinberg-Shemer, Orna, Yacobovich, Joanne, Noy-Lotan, Sharon, Dgany, Orly, Krasnov, Tanya, Barg, Assaf, Landau, Yuval E, Kneller, Katya, Somech, Raz, Gilad, Oded, Brik Simon, Dafna, Orenstein, Naama, Izraeli, Shai, Del Caño-Ochoa, Francisco, Tamary, Hannah, Ramón-Maiques, Santiago

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Alpha-Thalassemia Carrier due to –α3.7 Deletion: Not So Silent von Gilad, Oded, Steinberg-Shemer, Orna, Dgany, Orly, Krasnov, Tanya, Noy-Lotan, Sharon, Tamary, Hannah, Yacobovich, Joanne

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Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel von Yeshareem, Lital, Yacobovich, Joanne, Lebel, Asaf, Noy‐Lotan, Sharon, Dgany, Orly, Krasnov, Tanya, Berger Pinto, Galit, Oniashvili, Nino, Mardoukh, Jacques, Bielorai, Bella, Laor, Ruth, Mandel‐Shorer, Noa, Ben Barak, Ayelet, Levin, Carina, Asleh, Mahdi, Miskin, Hagit, Revel‐Vilk, Shoshana, Levin, Dror, Benish, Marganit, Zuckerman, Tsila, Wolach, Ofir, Pazgal, Idit, Brik Simon, Dafna, Gilad, Oded, Yanir, Asaf David, Goldberg, Tracie Alison, Izraeli, Shai, Tamary, Hannah, Steinberg‐Shemer, Orna

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Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome von Yanir, Asaf D., Krauss, Aviva, Stein, Jerry, Steinberg‐Shemer, Orna, Gilad, Oded, Lotan, Sharon Noy, Dgany, Orly, Krasnov, Tatyana, Kodman, Yona, Feuerstein, Tamar, Mardoukh, Jacques, Fishman, Hila, Geron, Ifat, Yacobovich, Joanne, Tamary, Hannah, Birger, Yehudit, Avrahami, Galia, Izraeli, Shai, Birenboim, Shlomit Barzilai

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Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias von Shefer Averbuch, Noa, Steinberg‐Shemer, Orna, Dgany, Orly, Krasnov, Tanya, Noy‐Lotan, Sharon, Yacobovich, Joanne, Kuperman, Amir A., Kattamis, Antonis, Ben Barak, Ayelet, Roth‐Jelinek, Batia, Chubar, Evgeni, Shabad, Evelyn, Dufort, Gustavo, Ellis, Martin, Wolach, Ofir, Pazgal, Idit, Abu Quider, Abed, Miskin, Hagit, Tamary, Hannah

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Molecular diagnosis of α‐thalassemia in a multiethnic population von Gilad, Oded, Shemer, Orna Steinberg, Dgany, Orly, Krasnov, Tanya, Nevo, Michal, Noy‐Lotan, Sharon, Rabinowicz, Ron, Amitai, Nofar, Ben‐Dor, Shifra, Yaniv, Isaac, Yacobovich, Joanne, Tamary, Hannah

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