1) hereditary leukonychia totalis
遗传性全白甲
1.
KLF7 and CPO gene mutation in a pedigree with hereditary leukonychia totalis;
遗传性全白甲家系的KLF7和CPO基因突变分析
2.
Keratin 17 gene mutation in a pedigree with hereditary leukonychia totalis;
遗传性全白甲一家系角蛋白17基因突变的研究
3.
CRYGA,CRYGB,CRYGC and CRYGD gene mutation in a pedigree of hereditary leukonychia totalis;
遗传性全白甲一家系的CRYGA、CRYGB、CRYGC和CRYGD基因突变分析
2) inherited cataract
遗传性白内障
1.
Current research in inherited cataract genes and molecular mechanism;
遗传性白内障致病基因及其机制的研究进展
4) genetic leukoencephalopathy
遗传性白质脑病
1.
Thoughts about the diagnosis of genetic leukoencephalopathy
遗传性白质脑病的诊断思路
2.
Neuroimaging characteristics of genetic leukoencephalopathy
遗传性白质脑病的神经影像学特点
5) alpha-fetoproteins/ genetics
甲胎蛋白类/遗传学
6) aceruloplasminia
遗传性铜蓝蛋白缺乏症
1.
Wilson’s disease,aceruloplasminia and Menkes syndrome all demonstrate low serum levels of ceruloplasmin.
肝豆状核变性、遗传性铜蓝蛋白缺乏症和Menkes综合征均可表现为血浆铜蓝蛋白降低。
补充资料：白甲军
1.五代时淮南农民起义军。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条