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TranslationMobile

伴性的,x連鎖的,性連鎖遺傳
伴性的,伴x染色體的,性連鎖的
性連鎖的

"x" in Chinese : vt. (x-ed, x'd x-ing, x'ing) ...
"link" in Chinese : n. 火把，火炬。
"recessive x-linked ichthyosis" in Chinese : x連鎖隱性遺傳魚鱗病
"x-linked adrenoleukodystrophy" in Chinese : 鏈鎖腎上腺腦白質(zhì)營養(yǎng)不良
"x-linked agammaglobulinemia" in Chinese : x-染色體連鎖的無丙球蛋白血癥; x連鎖無丙種球蛋白血癥,嬰兒伴性無丙種球蛋 ...
"x-linked asexual dwarfism" in Chinese : x連鎖性性征不發(fā)育侏儒癥
"x-linked copper deficiency" in Chinese : x-連鎖銅缺乏
"x-linked cutis laxa" in Chinese : x連鎖遺傳皮膚松垂
"x-linked disease" in Chinese : x染色體連鎖疾病; 連鎖疾病
"x-linked dominant" in Chinese : x伴性顯性遺傳
"x-linked dominant inheritance" in Chinese : x連鎖顯性遺傳; 連鎖顯性遺傳
"x-linked dominant xd" in Chinese : x伴性顯性遺傳
"x-linked enzyme deficiency" in Chinese : 伴性酶缺陷
"x-linked gama globulinemia" in Chinese : 性聯(lián)無γ球蛋白血癥; 性聯(lián)無球蛋白血癥
"x-linked gene" in Chinese : 連基因

Examples

Inhibition of ovarian cancer growth by small interfering rna targeting x - linked inhibitor of apoptosis gene
對卵巢上皮性癌細胞生長的影響
Mutation detection of abcd1 gene in the molecular diagnosis of x - linked adrenoleukodystrophy by denaturing hplc
法在腎上腺腦白質(zhì)營養(yǎng)不良分子診斷中的應(yīng)用
Her team focused on a particular protein involved in the nf - kappa b pathway called the " x - linked inhibitor of apoptosis " ( xiap )
她的小組集中于包含在nf - b通路中稱為x樣凋亡抑制蛋白（ xiap ）的一個特別的蛋白。
Pcr - based analysis method was carried out in the following study . dna amplification by pcr in cgg repeats were performed on 154 people as normal control ( 73 males and 81 females ) and 23 members from four x - linked mental retardation ( xlmr ) families . after electrophoresed on a 6 % - denaturing polyacrylamide gel ( acr : bis = 19 : l ) , genotypes of the objects were determined by analyzing pcr products
本研究采用較以往更為簡便有效的pcr技術(shù)方法，對隨機抽取的154人的正常群體（男性73人、女性sl人）及來自四個智力低下家系的23名成員進行了fmr基因cgg重復(fù)序列的擴增，利用變性聚丙烯酸胺凝膠電泳技術(shù)對不同等位基因類型進行分離和統(tǒng)計。
Fxs is characterized by x - linked mental retardation with additional features such as a long face with large protruding ears , macroorchidism , and eye - gaze avoidance etc . fxs is associated with a fragile site , designated fraxa ( fragile site , x chromosome , a site ) , at xq27 . 3 near the end of the long arm
其主要臨床特征為智力低下、特殊的外貌特征(包括長臉、大耳廓、下頜突出、巨頭、腭弓高、大睪丸等) 、行為及認知障礙、多動、注意力難集中以及孤獨、自閉等癥狀。