被遗传的

By using the Neighbor-joining method, a dendrogram was obtained based on genetic distances. The bootstrap values were evaluated for each crunode of the dendrogram by means of bootstrap test. The results showed that the mean heterozygosity of the whole native egg-typing duck breeds population was lower than those of native chicken breeds and goose breeds, suggesting that the genetic diversity in those duck breeds population is relativly rare and should be strengthened. The rank of the heterozygosity was consistent with that of the polymorphism information content. The results of the genetic distances between them indicated that the differentiation occurred long time ago. In the dendrogram, Weishan pocked, Youxian pocked, Huainan pocked, Guangxi pocked and Jingjiang pocked were classified into one goup, Chaohuand Enshi pocked were the second group, Liancheng white, Putian black, Jinding, Shanma, Sansui and Shaoxing were the flnra grong.

结果表明：我国所有蛋鸭品种全部群体的平均杂合度较低，其遗传多样性相对贫乏，各保种场要加强多样性的保护；各品种的平均多态信息含量的高低与群体平均杂合度的顺序完全一致；遗传距离的计算说明了13个品种的遗传距离较远，分化时间较长；13个地方蛋鸭品种被聚类为3个类，微山麻鸭、攸县麻鸭、淮南麻鸭、广西小麻鸭、荆江麻鸭聚为一类；巢湖鸭和恩施麻鸭聚为一类；福建省的鸭种连城白鸭、莆田黑鸭、金定鸭、山麻鸭与三穗鸭、绍兴鸭聚为一类。

Mongolian gerbil has been applied in many branches of life science, which is thought of as many a functional laboratory animal.

长爪沙鼠在生命科学诸多领域已得到广泛应用，是一种正在被国内外开发的"多功能性"实验动物，但有关长爪沙鼠的遗传研究甚少，其群体遗传结构尚不清楚。

Results: Osteopetrosis is a group of rare, heritable disorders of the skeleton characterized by increased bone density with typical X-ray manifestation. It can be divided into autosomal recessive osteopetrosis and autosomal dominant osteopetrosis. The prognosis vary greatly in different clinical type.

结果：石骨症是罕见的家族性先天性骨疾病，以骨密度增高为主要表现，分常染色体显性遗传和常染色体隐性遗传，分型不同，临床表现不同，X线有特征性改变，治疗上以对症治疗为主，造血干细胞移植被用于治疗本病。

Genetically, IV is thought to be an autosomal dominant disorder with virtually complete penetrance.

遗传特征上，寻常型鱼鳞病被认为是一种完全外显的常染色体显性遗传疾病。

Just as Tay-Sachs has almost been wiped out in the decades since Ashkenazi Jews have tested themselves for the gene, a universal carrier screen, combined with preimplantation genetic diagnosis for carrier couples who want biological children, will eliminate a hundred others.

正如在Ashkenazi犹太人对自己进行基因试验后，Tay-Sachs疾病在数十年间几乎就被全部消灭一样，一种普遍的携带者筛查并结合那些希望获得亲生子女的夫妇们进行植入前遗传诊断将消灭众多其它遗传疾病。

Telegony is a theory in heredity, now discredited but widely believed until the late 19th century, holding that offspring can inherit the characteristics of a previous mate of one or both parents.

先父遗传是一种遗传上的理论，现今它被证明不真实，但是直到19世纪晚期，它还广泛地被相信和接受。这个理论是说，后代能继承父母双方中一方的前任伴侣的特徵。

Telegony is a theory in heredity , now discredited but widely believed until the late 19th century, holding that offspring can inherit the characteristics of a previous mate of the female parent; thus the child of a widowed or remarried woman might partake of traits of a previous husband.

先父遗传是一种遗传上的理论，现今它被证明不真实，但是直到19世纪晚期，它还广泛地被相信和接受。这个理论是说，后代能继承父母双方中一方的前任伴侣的特征，因此寡妇或再婚女人的子女会有她们前任丈夫的部分特征。

Male gametophytic selection is known as a powerful motivation in biological evolution, and is also considered as an important factor that influences genetic differentiation, variation and genetic diversity in plant.

雄配子体选择是影响植物遗传分化、演变和遗传多样性的重要因素，被认为是生物进化的有力动力。

There was great diversity index among genetic trait of 50 barley. The anomic trait used as tested materials was analyzed by cluster. Cluster analysis showed that 50 barley could be classified into 5 groups at the level of GD 3.28; The 50 barleys were analyzed by A-PAGE to study genetic diversity of hordein.

各农艺性状的遗传多样性指数都较大，具有丰富的遗传多样性；对供试材料的农艺性状进行聚类分析，50份大麦材料在遗传距离3.28时可被聚为5大类。

Diagnosis/testing. A diagnosis of ocular albinism is probable in the presence of congenital nystagmus, iris translucency, and significant hypopigmentation of the ocular fundus periphery in males with normal skin pigmentation and foveal hypoplasia, reduced visual acuity, and aberrant optic pathway projection, as demonstrated by crossed asymmetry of the cortical responses on visual evoked potential. X-linked inheritance is documented by either a family history consistent with X-linked inheritance or the presence of typical carrier signs (irregular retinal pigmentation and partial iris transillumination) in an obligate carrier female.

诊断/检测。对于皮肤色素沉着正常、中央凹发育不全、视敏度降低以及视径投射异常（VEP，表现为视觉诱发电位中皮层反应的交叉不对称）的男性患者，当存在先天眼球震颤、虹膜半透明以及显著的眼基底层边缘色素减退的症状时，可被疑似诊断为眼白化病。X连锁性遗传则以存在与X连锁遗传一致的家族病史，或在一个应当为携带者的女性中存在典型的携带者迹象（视网膜色素沉着不规则以及部分虹膜透射）而被确认。

I didn't watch TV last night, because it .

昨晚我没有看电视，因为电视机坏了。

Since this year, in a lot of villages of Beijing, TV of elevator liquid crystal was removed.

今年以来，在北京的很多小区里，电梯液晶电视被撤了下来。