Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Syndrome and RAD51[original query] |
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| The BCL2L10 Leu21Arg variant and risk of therapy-related myeloid neoplasms and de novo myelodysplastic syndromes. Leukemia & lymphoma 2014 Jul 55 (7): 1538-43. Fabiani Emiliano, Fianchi Luana, Falconi Giulia, Boncompagni Riccardo, Criscuolo Marianna, Guidi Francesco, La Brocca Antonella, Hohaus Stefan, Leone Giuseppe, Voso Maria Tere |
| Association between RAD51 gene polymorphism (-135G/C) and susceptibility of myelodysplastic syndrome and acute leukemia: evidence based on a meta-analysis. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Jan 35 (1): 615-21. He Ya-zhou, Hu Xin, Chi Xiao-sa, Zhang Yuan-chuan, Deng Xiang-Bing, Wei Ming-tian, Wang Zi-qiang, Zhou Yan-ho |
| A DNA repair variant in POLQ (c.-1060A > G) is associated to hereditary breast cancer patients: a case-control study. BMC cancer 2014 14 850. Brandalize Ana Paula Carneiro, Schüler-Faccini Lavínia, Hoffmann Jean-Sébastien, Caleffi Maira, Cazaux Christophe, Ashton-Prolla Patric |
| Polymorphisms of DNA repair genes are related to the pathogenesis of myelodysplastic syndrome. Hematological oncology 2014 Oct . Ribeiro Howard Lopes, de Oliveira Roberta Taiane Germano, Maia Allan Rodrigo Soares, Pires Ferreira Filho Luiz Ivando, de Sousa Juliana Cordeiro, Heredia Fabiola Fernandes, Magalhães Silvia Maria Meira, Pinheiro Ronald Feito |
| Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia-like phenotype, and no chromosome fragility. Molecular genetics & genomic medicine 2019 7 7 (9): e863. Keupp Katharina, Hampp Stephanie, Hübbel Annette, Maringa Monika, Kostezka Sarah, Rhiem Kerstin, Waha Anke, Wappenschmidt Barbara, Pujol Roser, Surrallés Jordi, Schmutzler Rita K, Wiesmüller Lisa, Hahnen Er |
| Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population. BMC medical genomics 2020 Feb 13 (1): 21. da Costa E Silva Carvalho Simone, Cury Nathalia Moreno, Brotto Danielle Barbosa, de Araujo Luiza Ferreira, Rosa Reginaldo Cruz Alves, Texeira Lorena Alves, Plaça Jessica Rodrigues, Marques Adriana Aparecida, Peronni Kamila Chagas, Ruy Patricia de Cássia, Molfetta Greice Andreotti, Moriguti Julio Cesar, Carraro Dirce Maria, Palmero Edenir Inêz, Ashton-Prolla Patricia, de Faria Ferraz Victor Evangelista, Silva Wilson Arau |
| Human mutational constraint as a tool to understand biology of rare and emerging bone marrow failure syndromes. Blood advances 2020 10 4 (20): 5232-5245. Oved Joseph H, Babushok Daria V, Lambert Michele P, Wolfset Nicole, Kowalska M Anna, Poncz Mortimer, Karczewski Konrad J, Olson Timothy |
| Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition. Genes, chromosomes & cancer 2020 Oct . Cavaillé Mathias, Uhrhammer Nancy, Privat Maud, Ponelle-Chachuat Flora, Gay-Bellile Mathilde, Lepage Mathis, Molnar Ioana, Viala Sandrine, Bidet Yannick, Bignon Yves-Je |
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