常染色体遗传,autosomal inheritance
1)autosomal inheritance常染色体遗传
英文短句/例句

1.Progress in the gene-related study on autosomal retinitis pigmentosa常染色体遗传型视网膜色素变性相关基因的研究进展
2.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
3.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。
4.Cytogenetical analysis on 218 cases with chromosomal abnormality218例染色体异常者的细胞遗传学分析
5.With pedigree analysis, the genetic mode of the disease in the family are autosomal dominant inheritance.据系谱分析,该疾病符合常染色体显性遗传方式。
6.Molecular Cytogenetic Detection of Minute Chromosomal Structural Abnormality on the Chromosomal Terminal Regions染色体末端微小结构异常的分子细胞遗传检测
7.The Study of Disease-Causing Genes of Autosomal Dominant Congenital Cataract;常染色体显性遗传白内障致病基因的研究
8.Laparoscopic Management of Autosomal Dominant Polycystic Kidney;常染色体显性遗传性多囊肾病的腹腔镜治疗
9.Preimplantation Genetic Diagnosis for Patients with Chromosome Structure Abnormalities;染色体异常者的胚胎植入前遗传学诊断研究
10.Human Population Genetic Structures Revealed by High Density Autosomal SNPs;高密度常染色体SNPs揭示的现代人群遗传结构
11.Application of autosomal STR genetic markers in siblings identification;常染色体STR遗传标记在同胞鉴定中的应用
12.Cytogenetic analysis on 1247 abnormal chromosome patients1247例染色体异常患者的细胞遗传学分析
13.Cytogenectical Analysis of 128 Cases abnormal karyotype128例异常染色体核型的细胞遗传学分析
14.Progress in treatment of autosomal dominant polycystic kidney disease常染色体显性遗传多囊肾病的治疗研究进展
15.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
16.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
17.HHT is an autosomal dominant disordercharacterized by vascular dysplasia.HHT是常染色体显性遗传性血管发育异常的一种疾病。
18.Analysis of the mutations of rhodopsin gene in autosomal dominant retinitis pigmentosa family常染色体显性遗传视网膜色素变性家系视紫红质基因突变分析
相关短句/例句

autosomal recessive常染色体隐性遗传
1.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
2.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
3.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。
3)autosomal recessive inheritance常染色体隐性遗传
4)autosomal dominant inheritance常染色体显性遗传
1.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。
2.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。
3.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。
5)autosomal dominant常染色体显性遗传
1.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
2.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
3.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。
6)haplotype of Y-STR常染色体STR遗传多态性
延伸阅读

常染色体常染色体autosome  在雌雄异体的个体中,性染色体以外的其他染色体。人体正常体细胞有22对常染色体。见“染色体”。