英语词汇“autosomal”的意思、用法、释义、翻译、读音、例句、短语、词组-英语词典

是什么意思

adj.

正染色体的，常染色体的；

英英释义

autosomal[ ,?:t?u's?um?l ]

adj.of or relating to an autosome
"autosomal gene"

学习怎么用

词组短语

autosomal dominant inheritance常染色体显性遗传

双语例句

用作形容词(adj.)

Xeroderma pigmentosum is an autosomal recessive disease.
着色性干皮病是一种常染色体的退行性疾病。

权威例句

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.
Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.
Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)
Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2).
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Di...

单词	autosomal
释义	autosomal 听听怎么读英 [??:t?'s??m?l] 美 [??t?'so?m?l] 是什么意思 adj. 正染色体的，常染色体的；英英释义 autosomal[ ,?:t?u's?um?l ] adj.of or relating to an autosome "autosomal gene" 学习怎么用词组短语 autosomal dominant inheritance常染色体显性遗传双语例句用作形容词(adj.) Xeroderma pigmentosum is an autosomal recessive disease. 着色性干皮病是一种常染色体的退行性疾病。权威例句 Mutations in PCSK9 cause autosomal dominant hypercholesterolemia Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID) Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2). A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Di...
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