autosomal
美 [??t?'som?l] 
英 [??:t?'s??m?l]
- adj.常染色體的
- 網絡遺傳特征為自體；正染色體；正染色體的
英漢解釋
例句
It is usually inherited as an autosomal dominant trait, although autosomal recessive and X-linked inheritance are seen less commonly.
人群中，大部分遺傳性白內障是外顯率較高的常染色體顯性遺傳，但也有X連鎖和常染色體隱性遺傳存在。
Spinal muscular atrophy in childhood is one of the most common neuromuscular disorders with an autosomal recessive mode of inheritance.
兒童型脊髓性肌萎縮癥是常見的遺傳性神經肌肉病，為常染色體隱性遺傳。
Multiple osteochondromas can occur either spontaneously or in an autosomal dominant disorder known as hereditary multiple exostoses .
多發骨軟骨瘤可能是自發，也可能是常染色體顯性遺傳疾病—遺傳性多發性外生骨疣病的表現。
They also found adermatoglyphia to be autosomal dominant, meaning only one parent needs to pass on the mutation for the child to show it.
他們也發現皮紋病是顯性遺傳，意味著只有一個父母將突變傳給孩子去顯現出來。
Genetic analysis indicated that the CVD character is controlled by an autosomal recessive gene with 100% penetrance.
遺傳分析表明，心血管疾病的性質是由一個常染色體隱性基因外顯率100%。
An aneuploid state in which a third homologous chromosome is present in addition to the normal autosomal pair is called trisomy.
除了正常染色體對以外，還存在有第二種同源染色體的非整倍體狀態，被稱為三體性。
This type of inheritance is called autosomal recessive inheritance.
這種被稱為常染色體隱性遺傳繼承。
It is a common occurrence in dogs and is thought to be a sex-limited autosomal recessive trait.
該疾病常發于犬，并被認為具有限性常染色體隱性遺傳特征。
Similar to other anxiety disorders, it may be inherited as an autosomal dominant trait.
與其它焦慮癥一樣，可能作為常染色體顯性性狀遺傳。
Objective: To investigate the clinical features of an autosomal recessive inherited ataxia pedigree and exclude known causal genes.
目的：探討常染色體隱性遺傳性共濟失調家系的臨床特征并排除已知的致病基因。
ABSTRACT: Objective To elucidate the pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris (IV).
摘要：目的研究一常染色體顯性遺傳尋常型魚鱗病家系的致病基因。
Recent studies have revealed mechanistic parallels between imprinted X-chromosome inactivation and autosomal imprinting.
最近的研究表明機械相似之處印跡X染色體失活和常印記。
Two rare, inherited forms have been reported in cattle, both characterized by autosomal recessive transmission.
兩個少見的遺傳形式報告了牛，這兩個特點是常染色體隱性傳染。
Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance.
結論：手掌小魚際區真實花紋可能屬于常染色體顯性遺傳。
Von Hippel-Lindau (VHL) disease is an autosomal, dominantly inherited, tumour syndrome.
希佩爾一林道（VHL）病是一種常染色體，顯性遺傳，腫瘤綜合征。
Dense incisors (din) is a new autosomal recessive mutation in the mouse that interferes with complete eruption of the incisors.
密集切牙（標準）是一種新的常染色體隱性基因突變的老鼠會干擾完成爆發門牙。
Certain autosomal translocations in the heterozygous state can be fully viable .
呈雜合子狀態的某些常染色體易位完全可以生活的。
Some members of the patients family were similarly affected and indicated an autosomal dominant trait of inheritance.
一些親屬亦有類似病癥，顯示是體顯性遺傳模式。
Congenital adrenal hyperplasia is a genetic disorder transmitted by autosomal recessive pattern.
先天性腎上腺增生癥是一種自體隱性遺傳病。
Results The inheritance pattern of the ADAAA family was autosomal dominant with complete penetrance.
結果該家系的遺傳模式為常染色體顯性遺傳，完全外顯。
Genetic counseling and ANKRD26 mutation analysis should be offered to patients with autosomal-dominant thrombocytopenia.
而且，也應向常染色體顯性血小板減少證患者提供遺傳咨詢和進行ANKRD26突變分析。
After full investigation of available data a suspected autosomal dominant inheritance pattern of PS could not be confirmed.
經充分調查后對現有數據懷疑常染色體顯性遺傳模式的PS都沒有得到證實。
Objective To detect mutation in the rhodopsin gene ( RHO ) in a Chinese family with autosomal dominant retinitis pigmentosa (ADRP).
目的確定常染色體顯性遺傳視網膜色素變性家系的致病基因及其突變位點，并研究其臨床表型。
Objective To analyze the occurrence character of autosomal dominant familial polycystic kidney.
目的分析常染色體顯性遺傳多囊腎的發病特點。
Harlequin ichthyosis (HI)is a severe subtype of autosomal recessive congenital ichthyoses (ARCI).
丑角樣魚鱗病是常染色體隱性遺傳性魚鱗病的一種嚴重亞型。
The condition is passed along genetically as an autosomal dominant trait.
條件是家族的遺傳作為常染色體顯性遺傳特征。
Autosomal trisomy is a common cause of human miscarriage, malformations and learning disability.
常染色體是人類的共同事業流產，畸形和學習障礙。
CBAS usually occurred by autosomal recessive inheritance, due to various enzymes defect in bile acid synthesis.
CBAS多屬于常染色體隱性遺傳，由膽汁酸合成過程中的酶缺陷所致。
The disease is autosomal-recessive and linked to the X-chromosome, so that men whose mothers are carriers of the gene manifest the disease.
該病屬常染色體隱性遺傳，與X-染色體關聯，所以，母親是基因攜帶者的男性表現為發病。
This disorder is inherited as an autosomal dominant trait .
本病作為常染色體顯性傳遞。
Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.
牙本質形成不良是一種體染色體顯性遺傳的中胚層缺陷。
With pedigree analysis, the genetic mode of the disease in the family are autosomal dominant inheritance.
據系譜分析，該疾病符合常染色體顯性遺傳方式。
The Alzheimer in this ancestry appears as autosomal dominant genetic disease .
阿爾茨海默病在本家系中顯示為常染色體顯性遺傳。
A Six-generation Family with Autosomal Dominant Deafness Passed Along: Possibly A New Locus?
六代相傳顯性遺傳耳聾大家系：一個可能的新基因座？
We describe twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia (SED) tarda.
我們描述與常染色體顯性脊柱，骨骺發育不良的孿生兄弟，父親（SED）的菌。
A family tree study revealed an autosomal mode of inheritance with good penetrance.
家庭樹研究發現染色體模式的繼承與良好的外顯。
WD is a common autosomal recessive inherited neuropathy, whose only pathogenic gene is ATP7B.
WD是神經科較為常見的常染色體隱性遺傳病，其唯一致病基因為ATP7B基因。
Inheritance is autosomal dominant in almost all cases.
常染色體顯性遺傳是在幾乎所有情況下。
Dermoid sinus is a genetic, autosomal skin condition in dogs.
皮竇是一種犬類的常染色體遺傳病。
We characterized a 3 generation family with autosomal dominant aniridia.
我們收集到一個連續3代發病的常染色體顯性遺傳的無虹膜癥家系。
