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搜索结果: 1-5 共查到医学遗传学 Type 2相关记录5条 . 查询时间(0.141 秒)
New research funded by the British Heart Foundation (BHF) and the Medical Research Council (MRC) has today revealed that genetic testing provides no real help in predicting the risk of developing type...
A 23 year-old man who was first seen in April 1996 gave a 8 year history of low back pain. This patient was treated with various antiinflamatory drugs for recent years. Father, mother and other sibshi...
Trichorhinophalangeal syndrome type I (TRPS I) is a rare complex genetic disorder characterized by sparse, slow growing hair, a bulbous pear-shaped nose, clinobrachydactyly and radiographically cone-s...
摘要阿尔茨海默类痴呆(AD)是老年痴呆中最常见的一种,它以渐进性的神经功能退化并伴随着整体认知能力的下降为特征。早发性AD主要是由β-淀粉样前体蛋白(APP)基因和早老素基因突变引起,而与晚发性AD发病明显相关的只有载脂蛋白E-ε4 ( APOE-ε4)等位基因。但是APOE-ε4等位基因对AD发病既非充分又非必要,而且只能解释少于50%的AD的遗传变异。所以有必要进一步寻找与AD的关联基因。 ...
27 April, 2007,Scientists from the Peninsula Medical School and the University of Oxford have identified three new genes that predispose individuals to develop type 2 diabetes. This research, which fo...

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