Erratum: A reply to community genetics: 1998-2009... and beyond [0.03%]
社区遗传学：1998-2009……以及更远时期的纠错评论回复
Ron L Zimmern
Ron L Zimmern
Published Erratum
Journal of community genetics. 2010 Dec;1(4):205. DOI:10.1007/s12687-010-0031-z 2010
Ron L Zimmern
Ron L Zimmern
Wolf H Rogowski,Scott D Grosse,Jürgen John et al.
Wolf H Rogowski et al.
The use of predictive genetic tests is expanding rapidly. Given limited health care budgets and few national coverage decisions specifically for genetic tests, evidence of benefits and harms is a key requirement in decision making; however,...
Development of a questionnaire for evaluating genetics education in general practice [0.03%]
全科医生遗传学教育评价问卷的制定
Anna Flouris,Graeme Hawthorne,Maryanne Aitken et al.
Anna Flouris et al.
To support developments in genetics education, we constructed the GPGeneQ questionnaire to assess skills required for the practice of genetics by general practitioners (GPs). We describe the process of developing and validating this questio...
Using a community of practice to develop standards of practice and education for genetic counsellors in Europe [0.03%]
利用实践社区来发展欧洲遗传咨询师的实践标准和教育标准
Heather Skirton,Christine Patch,Marie-Antoinette Voelckel
Heather Skirton
The profession of genetic counselling is developing in Europe in response to the increased need for genetic healthcare. Standards of education and professional practice are needed to ensure that patients are provided with genetic counsellin...
Family matters: examining a multi-family group intervention for women with BRCA mutations in the scope of genetic counselling [0.03%]
遗传咨询中的家庭事务：在多家庭小组干预方面的BRCA突变女性案例分析
Alvaro Mendes,Raquel Chiquelho,Teresa Almeida Santos et al.
Alvaro Mendes et al.
The availability of family-centred services for women genetically at-risk for breast and ovarian cancer (BRCA) due to deleterious genetic mutations is still scarce, despite the distress that these women and their families may experience. Th...
A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka [0.03%]
印度、巴基斯坦和斯里兰卡β-地中海贫血突变的描述性特征分析
M L Black,S Sinha,S Agarwal et al.
M L Black et al.
Thalassaemia is a common and debilitating autosomal recessive disorder affecting many populations in South Asia. To date, efforts to create a regional profile of β-thalassaemia mutations have largely concentrated on the populations of Indi...
Influence of genetic variants in the apolipoprotein A5 and C3 gene on lipids, lipoproteins, and its association with coronary artery disease in Indians [0.03%]
载脂蛋白A5和C3基因多态性对中国人的血脂、冠状动脉疾病的影响及连锁不平衡分析
Aparna A Bhanushali,Bibhu R Das
Aparna A Bhanushali
Indians worldwide demonstrate a triad of elevated triglyceride (TG) with high low-density lipoprotein cholesterol and low high-density lipoprotein cholesterol levels. In the present study, we aim to investigate the effect of -1131T > C, -3A...
Prospective experience with contingent screening strategy for Down syndrome in Estonia [0.03%]
爱沙尼亚唐氏综合征筛查兼顾式策略的前瞻性研究体验
Kai Muru,Mari Sitska,Karin Asser et al.
Kai Muru et al.
The purpose of this study was to establish the first-trimester screening for Down syndrome (DS) in Estonia and to evaluate the potential of a contingent screening in the population of pregnant women. A prospective cohort study included non-...
Genetic diversity of hemoglobinopathies, G6PD deficiency, and ABO and Rhesus blood groups in two isolates of a primitive Kharia Tribe in Sundargarh District of Northwestern Orissa, India [0.03%]
印度奥里萨邦苏纳尔加尔区两个隔离的原始部落kharias群体的血红蛋白病、g6pd缺乏症以及abo和rh血型的基因多样性研究
R S Balgir
R S Balgir
Tribal communities constitute about 8.2% of the total population of India. Their health needs are even larger than elsewhere in India; this study investigates the genetic diversity in relation to hemoglobinopathies, G6PD deficiency and, ABO...