目的研究异烟肼乙酰化遗传型。
据报道很少一部分为常染色体隐性遗传型。
Rare autosomal recessive inheritance has also been described.
科学家称这种爪型为抗体微小颗粒的遗传型。
Scientists call this claw shape the antibody molecule's idiotype.
“狗有268个同人类类似的遗传型疾病，”Lee解释说。
"The dog has 268 genetic type diseases that are similar to those of humans," Lee explained.
以往对于人类的研究鉴定出了五个可导致遗传型黄疸的基因。
Previous research on humans identified five genes responsible for inherited forms of jaundice.
婴儿型多囊肾又叫常染色体隐性遗传型多囊肾，是两种多囊肾中的一种。
Infantile polycystic kidney disease and autosomal recessive polycystic kidney disease, is the two kind of polycystic kidney in a kind.
同时对12个具有不同抗性水平的水稻品种苗期的抗性表现进行了遗传型稳定性分析。
Stability of resistance of 12 rice varieties with different resistant levels in seedling stage was studied.
常染色体隐性遗传型多囊肾的病因主要是因为父母先天性的遗传，所以在婴儿期就开始发病。
Autosomal recessive polycystic kidney disease etiology is mainly because the parents with congenital genetic, so in infancy began to sicken.
将人类DNA——这个人类生命的遗传型版破解，是21世纪科学研究所面临的最大挑战之一。
Decoding human DNA, the inherited blueprint for each human life, is one of the biggest challenges facing science in the 21st century.
目的研究常染色体显性遗传型多囊肾病肾组织中细胞外基质和多囊蛋白-1的表达及与囊肿发生的关系。
Objective To study the expression of extracellular matrix and polycystin-1 in ADPKD and their relation to cyst formation.
植物嵌合体是由2种或者2种以上遗传型细胞组成的特殊的植物结构，它在西欧国家观赏植物产业中发挥着非常重要的作用。
The plant chimera contains at least 2 different genotypes in the shoot apex of plants and plays an important role in the ornamental plant market in Europe.
象这些结果所显示的一样，如果家庭环境有害因素的影响依赖于遗传型，那么遗传型-环境就能解释其对哮喘和相关病症巨大遗传可能性。
If the influence of the home environmental risk factors depends on genotype, as suggested by these results, genotype-environment explains the large heritability for asthma and related disorders.
结果发现散发型克雅氏病临床诊断病例143例(44.14%)，疑似诊断病例15例(4.63%)，遗传型克雅氏病病例10例(3.09%)，致死性家族型失眠症8例(2.47%)。
Results a total of 143 probable CJD cases (44.14%) and 15 possible CJD cases (4.63%), 10 genetic CJD cases (3.09%) and 8 fatal familial insomnia (FFI) cases (2.47%) were identified.
结果发现散发型克雅氏病临床诊断病例143例(44.14%)，疑似诊断病例15例(4.63%)，遗传型克雅氏病病例10例(3.09%)，致死性家族型失眠症8例(2.47%)。
Results a total of 143 probable CJD cases (44.14%) and 15 possible CJD cases (4.63%), 10 genetic CJD cases (3.09%) and 8 fatal familial insomnia (FFI) cases (2.47%) were identified.
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