遗传学的

In this review, we primarily focus on the behavioral-neuroendocrine mechanism of development of homosexuality from genetic, neuroendocrine neuroanatomical and behavioral studies.

本文主要从生物学角度出发，从遗传学、神经内分泌学、行为学和神经解剖学方面综述了同性恋发生的神经内分泌机制。

In this study,we have employed the genetic approaches and tools to investigate the potential functions of condensins and nucleolar proteins in gene silencing at rDNA region in fission yeast.

本研究中，我们主要采用遗传学方法和工具，研究了集缩素和一些核仁蛋白在调控裂殖酵母rDNA基因沉默中的潜在功能。

SYNTHESIS OF NEW SPECIES AND CYTOGENETIC STUDIES IN OLEIFEROUS BRASSICA——II.

芸苔属油菜植物的新种合成及其细胞遗传学研究——II。

Center for Ecology and Conservation Biology is primarily dedicated to education and research in ecology and conservation biology including paleoceanography, ecological economics, sensory biology, behavioral ecology of birds, behavioral ecology and insect sociobiology, evolutionary biology, ichthyology, forest ecology and biogeochemistry, mammalian population genetics, etc.

生态学与保护生物学中心致力于生态学与保护生物学的教学与研究，其研究领域包括古海洋学，生态经济学，感官生物学，鸟？？？？？行为生态学，行为生态学和昆虫社会生物学，进化生物学，鱼类学，森林生态学和生物地理化学，哺乳动物遗传学等。

Review on inheritance of pesticide resistance in phytophagous spider mites.

武予清，刘芹轩， 1994。植食叶螨抗药性遗传学研究的进展。

A sample of 285 Khmu (141 males, 144 females) was investigated on 7 human population genetic characters, including nasal profile, nostril type, chin type, pollical type, palmar digital fomula, tongue rolling and hand clasping.

调查了我国克木人285例（男为141例，女为144例）的鼻梁侧面观、鼻孔形状、下颏类型、拇指类型、环食指长、卷舌、扣手共7项人类群体遗传学经典指标。

The field of this course mainly studies the chromosomal disorder, single gene disorder,polygenetic disorders,genetic diagnosis and counseling.

本课程的五个重要内容包括染色体病、单基因遗传病、多基因遗传病、遗传学诊断与遗传咨询。

Genetic studies have been performed on the hereditary diseases of disseminated superficial actinic porokeratosis, familial progressive hyperpigmentation and triphalangeal thumb-polysyndactyly syndrome by linkage analysis and sequencing.

本研究通过连锁分析和直接测序的方法，分别对播散性浅表性光化性汗孔角化症、家族性进行性色素过度沉着症和拇指三指节多指并指多掌骨畸形这三种疾病进行了遗传学分析。

Genetic studies have been performed on the hereditary diseases of disseminated superficial actinic porokeratosis, familial progressive hyperpigmentation and triphalangeal thumb-polysyndactyly syndrome by linkage analysis and sequencing.

中文摘要本研究通过连锁分析和直接测序的方法，分别对播散性浅表性光化性汗孔角化症、家族性进行性色素过度沉着症和拇指三指节多指并指多掌骨畸形这三种疾病进行了遗传学分析。

Objective To characterize the clinical and genetic features of punctate palmoplantar keratoderma in 40 cases from 5 Chinese Han families.

目的了解中国汉族人点状掌跖角化病（punctate，palmoplantar keratoderma）的临床表型和遗传学特点。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。