Nijmegen breakage syndrome
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Last Posted: Aug 04, 2023
- Germline Genetic NBN Variation and Predisposition to B-cell Acute Lymphoblastic Leukemia in Children.
Jun Yang, et al. Research square 2023 0 - Newborn screening for severe combined immunodeficiency: The results of the first pilot TREC and KREC study in Ukraine with involving of 10,350 neonates.
Boyarchuk Oksana et al. Frontiers in immunology 2022 13999664 - Spectrum of Hematological Malignancies, Clonal Evolution and Outcomes in 144 Mayo Clinic Patients with Germline Predisposition Syndromes.
St Martin Emma et al. American journal of hematology 2021 - Association of Nijmegen Breakage Syndrome 1 Genotypes With Bladder Cancer Risk.
Chen Meng, et al. Anticancer research 2020 4 (4) 2011-2017 - Chromosome instability syndromes.
Taylor A Malcolm R et al. Nature reviews. Disease primers 2019 Sep 5(1) 64 - Association of Single-Nucleotide Polymorphisms in Monoubiquitinated FANCD2-DNA Damage Repair Pathway Genes With Breast Cancer in the Chinese Population.
Chen Fei-Yu, et al. Technology in cancer research & treatment 2018 1 1533033818819841 - NBS1 rs2735383 polymorphism is associated with an increased risk of laryngeal carcinoma.
Hu Xinmei, et al. BMC cancer 2018 0 (1) 175 - A non-synonymous polymorphism in NBS1 is associated with progression from chronic hepatitis B virus infection to hepatocellular carcinoma in a Chinese population.
Zhen Ya'nan, et al. OncoTargets and therapy 2018 0 563-569 - Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders.
Walsh Michael F et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2017 Jun 23(11) e23-e31 - Contribution of Double-strand Break Repair Gene Nijmegen Breakage Syndrome 1 Genotypes, Gender Difference and Smoking Status to Taiwanese Lung Cancer.
Chuang Chin-Liang, et al. Anticancer research 2017 0 (5) 2417-2423
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