| 释义 |
au·to·som·al 英,ɔtə'soməl美,ɔtə'soməl 高ＳCOCA⁸²²⁰²BNC⁸⁶⁶⁶⁰⁺⁹iWeb²⁴²¹⁶
基本英英搭配派生词例句例句
adj.常染色体的¹⁰⁰
生物
Adjective:
of or relating to an autosome;autosomal gene autosomal dominant inheritance常染色体显性遗传…autosomal inheritance常染色体遗传,正染色…autosomal abnormalities常染色体异常…autosomal gene常染色体基因…autosomal dominant常染色体显性…autosomal recessive inheritance常染色体隐性遗传…autosomal recessive常染色体隐性遗传…
Ppseudoautosomala.假体染色体
形容词59%,名词41%
用作形容词Xeroderma pigmentosum is anautosomalrecessive disease.着色性干皮病是一种常染色体的退行性疾病。 An investigation of a genetic Blepharostenosis family was reported. 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。 cnki
FHCM is a heterozygote autosomal dominant disease, and the incidence rate in male is obvious higher than that in female.
属杂合子常染色体显性遗传性疾病，男性患病率高于女性。 cnki
It is shown that the mean relative lengths and centromeric indices of autosomal SCs agree closely with those of mitotic chromosomes.
结果表明，常染色体联会复合体的相对长度和着丝点指数与体细胞染色体的相应参数具有很好的吻合性。 cnki
The results indicate that psoriasis is of autosomal dominant inheritance and incomplete phenotype.
认为银屑病属于常染色体显性遗传，伴不全表现。 cnki
Trapped Neutrophil Syndrome is an autosomal recessive disease which results in mature neutrophils being unable to migrate from the bone marrow into the blood.
遗传性嗜中性白血球减少症是一种常染色体隐性遗传疾病，该疾病导致成体中性粒细胞无法从骨髓迁移到血液中。 goumin
Conclusion: LP is an autosomal recessive disease, and the mutation of pathogenic gene of LP is rare in Chinese people.
结论： LP是一种罕见的常染色体隐性遗传病，中国人群中其致病基因的突变频率很低； cnki
Mutations in the cardiac sodium channel gene SCN5A also cause cardiac conduction disease and autosomal recessive sick sinus syndrome SSS.
心脏钠离子通道基因 SCN5A的突变也可导致心脏传导疾病和常染色体隐性病态窦房结综合征 SSS。 cnki
Neurofibromatosis is one of autosomal- dominant neurogenetic diseases with relatively low incidence.
神经纤维瘤病是一常染色体显性遗传性疾病，临床上较为少见。 dictall
Objective To discuss the probability of siblings identification by autosomal short tandem repeat STR.
目的探讨常染色体 STR遗传标记用于鉴定两个体同胞关系的可行性。 cnki
Objective To evaluate the role of homozygosity mapping in the fine mapping of the genes responsible for the rare autosomal recessive diseases.
目的探讨纯合子定位法在罕见常染色体隐性遗传病致病基因精确定位中的作用。 cnki
Objective To explore the clinical features of autosomal recessive juvenile Parkinson disease AR- JP.
目的探讨常染色体隐性遗传性青少年型帕金森病 AR- JP的临床特征。 cnki
Objective To investigate the etiology, pathology and genetic factors of an autosomal dominant hereditary disorder polycystic kidney.
目的通过一个家系分析，探讨常染色体显性遗传性多囊肾疾病的病因学、病理学、遗传学因素。 cjrh
Objective: To elucidate the molecular mechanism of neurofibromatosis type2NF2 with autosomal dominant inheritance disease in a Chinese kindred.
目的：探讨中国人常染色体显性遗传2型神经纤维瘤病的基因突变和分子诊断。 cnki
Pedigree analysis was compatible with law of autosomal dominant inheritance.
家系图谱分析符合常染色体显性遗传规律。 cnki
The disease is autosomal- recessive and linked to the X- chromosome, so that men whose mothers are carriers of the gene manifest the disease.
该病属常染色体隐性遗传，与 X-染色体关联，所以，母亲是基因携带者的男性表现为发病。 yeeyan
They also found adermatoglyphia to be autosomal dominant, meaning only one parent needs to pass on the mutation for the child to show it.
他们也发现皮纹病是显性遗传，意味着只有一个父母将突变传给孩子去显现出来。 kle100
Autosomal recessive inheritance was difficult to be evaluated because of few families remained.
常染色体隐性遗传因剩下的家系样本太少，难以预测； cnki |