父母的DNA序列是临床基因组学中至关重要的家族病史。 - Suppr

Suppr

超能文献

Parental DNA sequence is critical family history in clinical genomics.

作者信息

Murray Michael F

机构信息

Geisinger Health System, Forty Fort, Pennsylvania, USA.

出版信息

Genet Med. 2016 Jul;18(7):675-7. doi: 10.1038/gim.2015.177. Epub 2016 Jan 14.

DOI:10.1038/gim.2015.177

PMID:26765341

Abstract

摘要

相似文献

Parental DNA sequence is critical family history in clinical genomics.父母的DNA序列是临床基因组学中至关重要的家族病史。

Genet Med. 2016 Jul;18(7):675-7. doi: 10.1038/gim.2015.177. Epub 2016 Jan 14.

Taking a medical history in childhood illness: representations of parents in pediatric texts since 1850.记录儿童疾病的病史：1850年以来儿科文本中父母的形象

Bull Hist Med. 2005 Fall;79(3):393-429. doi: 10.1353/bhm.2005.0105.

Family pain history predicts child health status in children with chronic rheumatic disease.家族疼痛史可预测慢性风湿性疾病患儿的健康状况。

Pediatrics. 2001 Sep;108(3):E47. doi: 10.1542/peds.108.3.e47.

Family history: still relevant in the genomics era.家族史：在基因组学时代仍然重要。

Cleve Clin J Med. 2012 May;79(5):331-6. doi: 10.3949/ccjm.79a.11065.

Parental hypercholesterolemia and family medical history as predictors of hypercholesterolemia in their children.父母高胆固醇血症及家族病史作为其子女高胆固醇血症的预测因素。

Arch Argent Pediatr. 2019 Feb 1;117(1):41-47. doi: 10.5546/aap.2019.eng.41.

How accurate are parental chronic pain histories provided by offspring?子女提供的父母慢性疼痛病史有多准确？

Pain. 2005 Jun;115(3):390-397. doi: 10.1016/j.pain.2005.03.017.

Assessing parental history of hypertension: father (and mother) knows best!

Psychophysiology. 1998 May;35(3):341-3. doi: 10.1017/s0048577298000833.

Parent-child agreement and prevalence estimates of diagnoses in childhood: direct interview versus family history method.亲子协议与儿童期诊断的患病率估计：直接访谈法与家族史法

Int J Methods Psychiatr Res. 2009 Jun;18(2):96-109. doi: 10.1002/mpr.281.

Modification of second cancer risk after malignant melanoma by parental history of cancer.恶性黑色素瘤后第二癌症风险受父母癌症病史的影响。

Br J Cancer. 2008 Aug 5;99(3):536-8. doi: 10.1038/sj.bjc.6604489. Epub 2008 Jul 15.

Is a parental history of coronary arterial disease in children as discriminating as their lipoprotein profile? Niño Jesus Group.儿童冠状动脉疾病的家族史与他们的脂蛋白谱一样具有鉴别意义吗？尼诺·耶稣研究小组。

Int J Cardiol. 1992 Sep;36(3):267-71. doi: 10.1016/0167-5273(92)90295-e.

本文引用的文献

Preliminary validation of a consumer-oriented colorectal cancer risk assessment tool compatible with the US Surgeon General's My Family Health Portrait.一种与美国卫生局局长的“我的家庭健康画像”兼容的面向消费者的结直肠癌风险评估工具的初步验证。

Genet Med. 2015 Sep;17(9):753-6. doi: 10.1038/gim.2014.179. Epub 2014 Dec 18.

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.基于遗传模式分析的以家庭为中心的诊断外显子组测序的增强效用：来自500个未选择的患有未确诊遗传病家庭的结果。

Genet Med. 2015 Jul;17(7):578-86. doi: 10.1038/gim.2014.154. Epub 2014 Nov 13.

Clinical exome sequencing for genetic identification of rare Mendelian disorders.用于罕见孟德尔疾病基因鉴定的临床外显子组测序

JAMA. 2014 Nov 12;312(18):1880-7. doi: 10.1001/jama.2014.14604.

Molecular findings among patients referred for clinical whole-exome sequencing.接受临床全外显子组测序的患者的分子研究结果。

JAMA. 2014 Nov 12;312(18):1870-9. doi: 10.1001/jama.2014.14601.

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.临床全外显子测序用于孟德尔疾病的诊断。

N Engl J Med. 2013 Oct 17;369(16):1502-11. doi: 10.1056/NEJMoa1306555. Epub 2013 Oct 2.

Family history: the three-generation pedigree.家族史：三代系谱。

Am Fam Physician. 2005 Aug 1;72(3):441-8.

The family history--more important than ever.家族病史——比以往任何时候都更重要。

N Engl J Med. 2004 Nov 25;351(22):2333-6. doi: 10.1056/NEJMsb042979.

Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases.杜氏肌营养不良症的携带者检测。来自对孤立病例的 obligatory 携带者和母亲的研究证据。（注：“obligatory carriers”不太明确准确中文表述，可根据具体医学背景进一步优化）

Arch Dis Child. 1979 Jul;54(7):534-7. doi: 10.1136/adc.54.7.534.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验