autosomal 中文意思是什麼
autosomal
解釋
正染色體的, 常染色體的-
Complex vertebral malformation ( cvm ), a lethal autosomal recessive inherited defect in holstein breed, was newly reported in demark
摘要荷斯坦奶牛脊柱畸形綜合征是近年新發現的一種常染色體隱性遺傳病，該病對純合子胎兒是致死性的。 -
This disorder is inherited as an autosomal dominant trait.
本病作為常染色體顯性傳遞。 -
Hemochromatosis can be primary ( the cause is probably an autosomal recessive genetic disease ) or secondary ( excess iron intake or absorption, liver disease, or numerous transfusions )
血色素沉著癥或可以是原發的（病因大概為常染色體隱性遺傳病） ，也可以是繼發的（過多的鐵攝取或吸收、肝臟疾病、大量輸血） 。 -
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。 -
Xeroderma pigmentosum is an autosomal recessive disease.
著色性干皮病是一種常染色體的退行性疾病。 -
This is tuberous sclerosis, an autosomal dominant condition characterized by mental retardation and seizures beginning early in life
結節性硬化癥，常染色體顯性遺傳，表現為智力低下、癲癇發作等。 -
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。 -
Autosomal dominant inheritance,
常染色體顯性遺傳 -
According to genetic analysis, this disease is caused by autosomal dominant inheritance
經過遺傳分析，認為該畸形屬常染色體顯性遺傳。 -
As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant
家族性腺瘤息肉病的遺傳方式是常染色體顯性遺傳。 -
Nevoid basal cell carcinoma syndrome, also known as gorlin syndrome, is an autosomal dominant inherited disorder which is characterized by the presence of multiple maxillary keratocysts, facial basal cell carcinomas and kinds of musculo - skeletal disturbances
摘要痣樣基底細胞癌綜合征是一種罕見的常染色體顯性遺傳疾病，以頜骨多發性角化囊腫，皮膚痣樣基底細胞癌及多種骨骼異常為主要臨床表現。 -
Autosomal recessive inheritance, ar
常染色體隱性遺傳 -
In the autosomal recessive condition, the parents are generally healthy ? we call them ‘ carriers. ’ the probability of them having a child with another affected child is 25 percent
對于常染色體隱性遺傳，父母表面上通常是正常的? ?我們稱之為「攜帶者」 。他們生育相同疾病小孩的幾率將是25 % 。 -
Wilson " s disease is the consequence of toxic accumulation of copper initially in the liver and later in extrahepatic sites, this disorder is inherited in autosomal recessive manner and is present in 1 in 30000 individuals in all populations
其中研究最多的是銅代謝異常所引起的wilson ' s病，這種病是常染色體隱性遺傳病，如果肝臟中銅濃度達到毒性水平，將引發急性肝炎，其發生率為三萬分之一。 -
Retroperitoneal laparoscopic cyst decompression in patients with autosomal dominant polycystic kidney disease
后腹腔鏡去頂減壓術治療成人型多囊腎 -
Genomic imprinting refers to parent - of - origin - dependent gene expression. the presence of imprinted gene can cause cells with a full parental complement of functional autosomal genes to specifically express one allele but not the other, resulting in monoalielic expression of imprinted loci
基因組印記是指一種依賴于親本的基因表達形式，它導致常染色體上的功能基因單一表達一個等位基因而不表達另一個等位基因，造成印記位點的單等位基因表達。 -
Now autosomal and y - chromosomal strs are widely researched and applied, while the x - str markers are not. because x chromosome has the character that the male transmits his x chromosome only to his daughter ( s ), it can provide more information than the autosomal does, particularly in complex cases of kinship testing
而在解決一些復雜的親緣關系案件（如單親父女關系的鑒定和缺乏雙親的姐妹親緣關系的鑒定）時，由於父親的x染色體具有隻傳給他的女兒（們）的遺傳特性，因此在解決此類案件時有常染色體所無法比擬的優點。
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