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Evaluating a CLL susceptibility variant in in families with multiple subtypes of hematological malignancies.

作者信息

Blackburn Nicholas B, Marthick James R, Banks Annette, Charlesworth Jac C, Marsden Katherine A, Lowenthal Ray M, Blangero John, Dickinson Joanne L

机构信息

South Texas Diabetes and Obesity Institute, School of Medicine, University of Texas Rio Grande Valley, Brownsville, TX.

Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia; and.

出版信息

Blood. 2017 Jul 6;130(1):86-88. doi: 10.1182/blood-2017-03-774232. Epub 2017 May 10.

DOI:10.1182/blood-2017-03-774232
PMID:28490571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5813724/
Abstract
摘要

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本文引用的文献

1
Discussing and managing hematologic germ line variants.讨论和管理血液学种系变异。
Blood. 2016 Nov 24;128(21):2497-2503. doi: 10.1182/blood-2016-06-716704.
2
Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.对慢性淋巴细胞白血病（CLL）家族进行全外显子组测序，发现整合素β2中的一种变异与疾病易感性相关。
Blood. 2016 Nov 3;128(18):2261-2263. doi: 10.1182/blood-2016-02-697771. Epub 2016 Sep 14.
3
Analysis of protein-coding genetic variation in 60,706 humans.对60706名人类的蛋白质编码基因变异进行分析。
Nature. 2016 Aug 18;536(7616):285-91. doi: 10.1038/nature19057.
4
Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.对霍奇金淋巴瘤高危家族进行全外显子组测序：鉴定KDR基因中的一个易感突变。
Haematologica. 2016 Jul;101(7):853-60. doi: 10.3324/haematol.2015.135475. Epub 2016 Jun 13.
5
A retrospective examination of mean relative telomere length in the Tasmanian Familial Hematological Malignancies Study.塔斯马尼亚家族性血液系统恶性肿瘤研究中平均相对端粒长度的回顾性分析。
Oncol Rep. 2015 Jan;33(1):25-32. doi: 10.3892/or.2014.3568. Epub 2014 Oct 24.
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Guidelines for investigating causality of sequence variants in human disease.人类疾病中序列变异因果关系研究指南。
Nature. 2014 Apr 24;508(7497):469-76. doi: 10.1038/nature13127.
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