1) dominant genetic disease
显性遗传病
2) Dominant inheritance
显性遗传
1.
We think that the vitiligo in the family history is caused by autosomal dominant inheritance.
作者认为该家系的白癜风为常染色体显性遗
2.
It was proved that the disease was congenital eyelid syndrome and autosomal dominant inheritance.
报道了一个遗传性小眼症家系的调查结果 ,该家系属于先天性睑裂狭小综合症 ,为常染色体显性遗传 。
3.
Owing to the influence of various complex factors,it is possible for the heterozygote of autosomal dominant inheritance to appear in different phenotypes.
由于各种复杂因素的影响,常染色体显性遗传的杂合子有可能出现不同的表现型,本文阐述了常染色体显性遗传的几种类型。
3) autosomal dominant
显性遗传
1.
Exclusive mapping for all known locus linked with autosomal dominant congenital cataract in a Chinese family;
常染色体显性遗传白内障一家系基因排除定位研究
2.
Linkage Mapping of the Two Chinese Family with Autosomal Dominant Retinitis Pigmentosa;
两个常染色体显性遗传视网膜色素变性家系连锁分析
3.
The family was tested for linkage analysis to two known autosomal dominant CFEOM loci on chromosome 12p11.
根据目前已知的两种常染色体显性遗传类型的CFEOM的遗传学位点 12p11 2 q12 (FEOM1)和 16q2 4(FEOM3 )选取微卫星进行连锁分析研究。
4) X sex-linked dominant hereditary disease
X染色体显性遗传病
5) autosomal dominant inherited disease
常染色体显性遗传病
1.
Background and objective: Neurofibromatosis, also called Multiple Neurofibroma, is an autosomal dominant inherited disease with multi-system injured because of nervous crest cells disdifferentiation.
背景和目的: 神经纤维瘤病(neurofibromatosis,NF)又称多发性神经纤维瘤,是源于神经嵴细胞分化异常而导致的多系统损害的常染色体显性遗传病,是常累及神经、肌肉、骨骼、内脏、皮肤的一种先天性发育不良疾病。
6) co dominant inheritanc
共显性遗传
补充资料：显性遗传
显性遗传
dominant inheritance
生物学术语。指一种遗传性状或遗传缺陷受显性基因控制的遗传方式。若显性基因位于常染色体上，则称为常染色体显性遗传。
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