基本释义:

性染色体遗传

网络释义

1)allosomal inheritance,性染色体遗传

2)chromosome heredity,染色体遗传

3)autosomal recessive,常染色体隐性遗传

4)autosomal recessive inheritance,常染色体隐性遗传

5)autosomal dominant inheritance,常染色体显性遗传

6)autosomal dominant,常染色体显性遗传

用法和例句

A study of DJ-1 gene in 3 pedigrees with autosomal recessive early-onset Parkinson s disease;

常染色体隐性遗传早发型帕金森病家系的DJ-1基因研究

Clinical features of autosomal recessive juvenile Parkinson disease;

常染色体隐性遗传性青少年型帕金森病的临床特征

Papillon-Lefèvre syndrome(PLS) is an extremely rare inherited disease as an autosomal recessive trait.

掌跖角化-牙周破坏综合征(PLS)是一种罕见的常染色体隐性遗传性疾病,其特点是手掌和脚掌部位的皮肤过度角化以及乳、恒牙过早脱落。

Most cases of this disease are proved to be autosomal dominant inheritance.

多囊卵巢综合征是女性常见病和多发病,其发生主要受遗传控制,多数证实本病是常染色体显性遗传,一些基因位点已被提出,包括CYP11A、胰岛素基因以及胰岛素受体附近区域,研究较为深入的是胰岛素受体附近区域,已被两项独立研究证实,但是位于染色体19P13。

According to genetic analysis, this disease is caused by autosomal dominant inheritance.

经过遗传分析,认为该畸形属常染色体显性遗传。

they are autosomal dominant inheritance,autosomal recessive inheriance,x-linked dominant inheritance,x-linked recessive inheritance,holandric inheritance,that is Y-linked inheritance,sex-influenced inheritance,sex-limited inheritance,and etc.

人类单基因病的遗传方式有常染色体显性遗传 ,常染色体隐性遗传 ;X伴性显性遗传 ,X伴性隐性遗传 ,Y伴性遗传 ;从性遗传和限性遗传等。

Relationship between genotype and phenotype of autosomal dominant polycystic kidney disease;

常染色体显性遗传性多囊肾病基因型与临床表型的关系

Progress in the research of disease genes in autosomal dominant retinitis pigmentosa;

常染色体显性遗传视网膜色素变性致病基因的研究进展

To screen mutation hot spots in two Chinese autosomal dominant con-genital cataract pedigrees.

【目的】对2个常染色体显性遗传先天性白内障中国家系进行基因突变热点筛查,以了解这两个家系的先天性白内障是否与文献报道的17个突变热点相关。

Analysis of Genetic Instability of Chromosome and HPV Infection in Human Cervical Carcinoma;

宫颈癌染色体遗传不稳定性及HPV感染状态分析

Studies on the Inheritance Law of 13/17 Robertsonian Translocation Chromosomes in the Domestic Pig

家猪13/17罗伯逊易位染色体遗传规律的研究

sex-limited autosomal dominant inheritance

性限常染色体显性遗传;限性常染色体显性遗传

The occurrence of a repeated section of genetic material in a chromosome.

染色体重复染色体中遗传物质段的重复出现

According to genetic analysis, this disease is caused by autosomal dominant inheritance.

经过遗传分析，认为该畸形属常染色体显性遗传。

Validation the Haplotype Polymorphisms of the DXS7424-DXS101 on X-chromosome;

X染色体STR单倍型DXS7424-DXS101遗传多态性

Cytogenetical analysis on 218 cases with chromosomal abnormality

218例染色体异常者的细胞遗传学分析

Chromosome map (genetic map) A diagram showing the order of genes along a chromosome.

染色体图谱（遗传学图谱）：显示染色体上基因顺序的图谱。

Genetic Behaviour of Thinopyrum intermedium Chromosome 2Ai-2 in Different Wheat Chromosome Substitution Backgrounds of Group 2

2Ai-2染色体在小麦部分同源染色体代换背景中的遗传

(genetics)an organism having a diploid set of chromosomes from each parent.

（遗传学）从双亲各得到两套染色体的有机体。

The Forensic Applications of Sex Chromosomes and Mtdna Genetic Markers;

性染色体及线粒体DNA遗传标记的法医学应用

Cytogenetical study on karyotype and ploidy of Acipenser dabryanus Dumeril

小体鲟染色体核型及倍性的细胞遗传学研究

The inheritance pattern of EDMD includes X-linked recessive, autosomal dominant and recessive modes.

其遗传方式为X-连锁隐性、染色体显性和隐性遗传。

The Genetic Polymorphism and the Structural Analysis of STR Loci of Miao Nationality in Yunnan Province

云南苗族常染色体STR遗传多态性及其遗传结构分析

Clinical genetics and gene mapping studies on a family with autosomal dominant congenital cataract

常染色体显性遗传性白内障一家系的临床遗传学及基因定位研究

These chromosomes are so simple that some geneticists prefer to call them chromonemes.

这些染色体结构简单，许多遗传学家喜欢称它们为染色丝。

Study on the Mutation in Chromosome Heterochromatic Region and its Genetic Effects

染色体异染色质区变异特征及其遗传效应的研究

Gene： Unit of heredity that occupies a fixed position on a chromosome.

基因:在染色体上占据固定位置的遗传单位。