autosomal信息详情
adj.常染色体的；正染色体的
autobiographic novel───自传体小说
dams auto───自动水坝
autobiographies crossword───自传纵横填字游戏
interrogatories to defendant auto accident───对被告车祸案的质询
beneficence justice autonomy───慈善司法自治
go auto───自动驾驶
phase difference auto focus───相位差自动对焦
antares auto-tune───心大星自动调谐
autobiographic poem───自传体诗
autoplastic behavior───自塑性行为
Dermoid sinus is a genetic, autosomal skin condition in dogs.───皮窦是一种犬类的常染色体遗传病。
Autosomal recessive inheritance was difficult to be evaluated because of few families remained.───染色体隐性遗传因剩下的家系样本太少，难以预测；
Genetic counseling. Cystinosis is inherited in an autosomal recessive manner.───胱氨酸病是以常染色体隐性方式遗传。
It is usually inherited as an autosomal dominant trait, although autosomal recessive and X-linked inheritance are seen less commonly.───人群中，大部分遗传性白内障是外显率较高的常染色体显性遗传，但也有X连锁和常染色体隐性遗传存在。
Spinal muscular atrophy in childhood is one of the most common neuromuscular disorders with an autosomal recessive mode of inheritance.───儿童型脊髓性肌萎缩症是常见的遗传性神经肌肉病，为常染色体隐性遗传。
Multiple osteochondromas can occur either spontaneously or in an autosomal dominant disorder known as hereditary multiple exostoses .───多发骨软骨瘤可能是自发，也可能是常染色体显性遗传疾病—遗传性多发性外生骨疣病的表现。
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。
Genetic analysis indicated that the CVD character is controlled by an autosomal recessive gene with 100% penetrance.───遗传分析表明，心血管疾病的性质是由一个常染色体隐性基因外显率100%。
An aneuploid state in which a third homologous chromosome is present in addition to the normal autosomal pair is called trisomy.───除了正常染色体对以外，还存在有第二种同源染色体的非整倍体状态，被称为三体性。
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.