伴性遗传

决定胫色性状的Id/id基因为伴性遗传，隐性基因id在纯合子时有个逐步表达的过程；

The Id / id allele that determines shank color demonstrates sex-linked inheritance , and the recessive id is expressed gradually in the homozygotes .

而性连锁遗传中，Y连锁伴性遗传和X连锁遗传，与实际调查不符，可排除这种遗传方式。

Autosomal recessive inheritance was difficult to be predicted because few family samples remained and Y-lined inheritance were not in accordance with the actual investigation , so sex-linked inheritance could be excluded .

许多伴性遗传疾病需在孕早期进行胎儿性别鉴定，报告一种不经Southern转移的分子杂交方法，即利用凝胶原位杂交法对早孕绒毛Y基因进行快速诊断。

The fetal sex should be detected in the early gestation for many inherited sex-linked diseases . One method of molecular hybridization , hybridized directly on agarose minigel without Southern transfer , was reported here to diagnose Y-gene from early gestational villi .

番鸭快慢羽基因频率及伴性遗传的研究

Study on the Inheritance of Feathering Gene type in Muscovy Duck

伴性遗传和泄殖腔鉴别法仍然是性别鉴定的主要方法；

Sex linked inheritance and cloaca sexing will still bethe main methods of sexualization ;

以上的结果可推测稻褐飞虱致害性可能属于伴性遗传。

The above results suggest that the inheritance of virulence of the brown planthopper may be sex-linked .

在这篇文章中，我们根据色盲伴性遗传规律，给出其马尔可夫链的权限概率分布

In this paper , we give limiting probability distribution of markov chain according to low of company sex heredity of color blindness

色盲及色弱是常见的伴性遗传病，主要是由视网膜上视锥细胞的变异或者缺失引起的。

Color blindness and color weakness is a common sex-linked genetic disease which is mainly caused by the variation or missing of cone cells in the retina .

在开始的时候，确认胎儿性别的超声波扫描和其它技术是作为诊断设备来帮助有伴性遗传的病人帮助孕育健康儿童（译者注：超声波技术有助于早期检测胎儿性别，以此可以知道孕妇是否可到健康婴儿），如血友病。

The ultrasound and other technologies that identify the sex of a fetus started out as diagnostic devices to help people with sex-linked diseases , such as haemophilia , conceive healthy children .

色盲是伴性隐性遗传疾病，男性发病率为女性的二十倍。高分辨超声在常染色体隐性遗传性多囊肾诊断中的价值

Colour Blindness is a sex-linked recessive trait 20 times more common in men than in women . High-resolution Ultrasonography in the Assessment of Autosomal Recessive Polycystic Kidney Disease

鹌鹑伴性羽色用于遗传实验教学的方法研究

Study on methods of sex-linked plumage color in quails for genetic experimental instruction

用华1与伴1组配的F1、F2及F1与亲本回交的14个组合作遗传分析，认为催青敏感性状由位于Z性染色体上的一个主基因控制，呈隐性的伴性遗传。

Genetic analysis was done on 14 hybridized forms of Hua-1 with Ban-1 , including F1 , F2 and F1 backcrossing with their parents . It is considered that the temperature sensitive characteris controlled by a major gene , located in Z chromosome , which shows recessive sexlinked inheritance .