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Monoclonal Gammopathy of Undetermined Significance.
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Inherited genetic susceptibility to monoclonal gammopathy of unknown significance.
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Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance.
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Pathogenic germ line variants in a prospective multicenter cohort of patients with multiple myeloma.
Blood Neoplasia. 2024 Oct 12;2(1):100045. doi: 10.1016/j.bneo.2024.100045. eCollection 2025 Feb.
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New horizons in our understanding of precursor multiple myeloma and early interception.
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Influence of structural racism on cancer health disparities: Tailoring measures relevant to multiple myeloma.
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Anthropometric traits and risk of multiple myeloma: differences by race, sex and diagnostic clinical features.
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Genome Instability in Multiple Myeloma: Facts and Factors.
Cancers (Basel). 2021 Nov 26;13(23):5949. doi: 10.3390/cancers13235949.
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Germline variants at SOHLH2 influence multiple myeloma risk.
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Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes.
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本文引用的文献

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Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
Nat Genet. 2011 Nov 27;44(1):58-61. doi: 10.1038/ng.993.
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Personal and family history of immune-related conditions increase the risk of plasma cell disorders: a population-based study.
Blood. 2011 Dec 8;118(24):6284-91. doi: 10.1182/blood-2011-04-347559. Epub 2011 Oct 13.
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Prostate cancer risk alleles and their associations with other malignancies.
Urology. 2011 Oct;78(4):970.e15-20. doi: 10.1016/j.urology.2011.05.035. Epub 2011 Aug 5.
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Initial genome sequencing and analysis of multiple myeloma.
Nature. 2011 Mar 24;471(7339):467-72. doi: 10.1038/nature09837.
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Familial monoclonal gammopathy: hyper-responsive B cells in unaffected family members.
Eur J Haematol. 2011 May;86(5):396-404. doi: 10.1111/j.1600-0609.2011.01593.x. Epub 2011 Mar 30.
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Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.
Blood. 2011 Feb 10;117(6):1911-6. doi: 10.1182/blood-2010-09-308205. Epub 2010 Dec 3.

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