青年中文autosomal的意思
autosomal中文翻譯：
adj.常染色體的；正染色體的
autobiographic novel───自傳體小說
dams auto───自動水壩
autobiographies crossword───自傳縱橫填字游戲
interrogatories to defendant auto accident───對被告車禍案的質詢
beneficence justice autonomy───慈善司法自治
go auto───自動駕駛
phase difference auto focus───相位差自動對焦
antares auto-tune───心大星自動調諧
autobiographic poem───自傳體詩
autoplastic behavior───自塑性行為
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。
Autosomal recessive inheritance was difficult to be evaluated because of few families remained.───染色體隱性遺傳因剩下的家系樣本太少，難以預測；
Genetic counseling. Cystinosis is inherited in an autosomal recessive manner.───胱氨酸病是以常染色體隱性方式遺傳。
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。
Objective To improve the operative treatment of autosomal dominant polycystic kidney disease(ADPKD).
Epidermolytic palmoplantar keratoderma , a rare autosomal dominant hereditary disease, is a keratinization disorder of palms and soles caused by mutation in the keratin 9 gene.
Congenital afibrinogenemia is a rare autosomal recessive disorder, characterized by the complete absence or extremely reduced level of fibrinogen.
Objective To elucidate the molecular mechanism of autosomal dominant neurohypophyseal diabetes insipidus in Chinese.
Citrin deficiency is inherited in an autosomal recessive manner.
Autosomal bivalents can be arranged in order of size, but unambiguous identification of individual bivalents is not possible.
This disorder is inherited as an autosomal dominant trait.
HHT is an autosomal dominant disordercharacterized by vascular dysplasia.
Result: ATD is an uncommon autosomal recessive hereditary disorder of osteochondrodysplasia.