染色體疾病 的英文怎麼說

中文拼音 [rǎnshǎitǐjíbìng]
染色體疾病 英文
chromosomal disease
  • 染 : Ⅰ動詞1 （用染料著色）dye 2 （感染） catch [contract] （a disease） 3 （沾染） acquire （a bad hab...
  • 色 : 色名詞[口語] （顏色） colour
  • 體 : 體構詞成分。
  • 疾 : Ⅰ名詞1 （疾病） disease; sickness; illness 2 （痛苦） suffering; pain; difficulty 3 （姓氏） a su...
  • 病 : Ⅰ名詞1 （疾病; 失去健康的狀態） illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • 染色體 : [生物學] chromosome染色體疾病 chromosomal disorders; 染色體異常 chromosome abnormality
  • 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
  • 疾病 : disease; illness; sickness; pathema
  1. The majority of aberrations are sporadic although on rare occasions a chromosomal disorder is directly inherited.

    盡管偶爾可見一種染色體疾病是直接遺傳的，但是大量的染色體異常是散發的。
  2. It refers to vaginal looseness, vaginal abnormal flavor, leucorrhea with red and white discharge, senile vaginitis, trichomonal vaginitis, colpomycosis, pruritus vulvae, pelvic inflammation, endometritis, appendagitis, cervical erosion, hysteromyoma, ovarian cyst, polypus, irregular menses, algomenorrhea and related complaints, excessive excretion, cervicitis, mycoplasma infection, endocrine disturbance and the symptoms caused by these diseases including pain in inferior belly, menoxenia, dysmenorrheal, pruritus vulvae, leucorrhea with abnormal flavor, gloomy vultus with moth - patch, etc

    適用於陰道鬆弛、陰道異味、赤白帶下、老年性陰道炎、滴蟲陰道炎、黴菌性陰道炎、外陰瘙癢、盆腔炎、子宮內膜炎、附件炎、宮頸糜爛、子宮肌瘤、卵巢囊腫、息肉、月經不調、痛經不適、分泌物過多，宮頸炎、支原體感染，內分泌失調以及這些疾病引起的下腹疼痛、月經不調、痛經、外陰瘙癢、白帶異味、面色灰暗黃褐斑等。
  3. Serviceable range it refers to vaginal looseness, vaginal abnormal flavor, leucorrhea with red and white discharge, senile vaginitis, trichomonal vaginitis, colpomycosis, pruritus vulvae, pelvic inflammation, endometritis, appendagitis, cervical erosion, hysteromyoma, ovarian cyst, polypus, irregular menses, algomenorrhea and related complaints, excessive excretion, cervicitis, mycoplasma infection, endocrine disturbance and the symptoms caused by these diseases including pain in inferior belly, menoxenia, dysmenorrheal, pruritus vulvae, leucorrhea with abnormal flavor, gloomy vultus with moth - patch, etc

    適用於陰道鬆弛、陰道異味、赤白帶下、老年性陰道炎、滴蟲陰道炎、黴菌性陰道炎、外陰瘙癢、盆腔炎、子宮內膜炎、附件炎、宮頸糜爛、子宮肌瘤、卵巢囊腫、息肉、月經不調、痛經不適、分泌物過多，宮頸炎、支原體感染，內分泌失調以及這些疾病引起的下腹疼痛、月經不調、痛經、外陰瘙癢、白帶異味、面色灰暗黃褐斑等。
  4. 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） 。
  5. 8p22 of human chromosome is an region with abundant disease - related genes. it is said that it is susceptible loci of hypertension and schizophrenia. the region is also the loci of oncogene and tumor su - pressor gene

    人染色體8p22區是疾病基因富含區域，有報道說該區域是高血壓、精神分裂癥等疾病的易感位點，也是癌基因和抑癌基因的研究熱點。
  6. 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。
  7. The topics include : structure and function of genes, chromosomes and genomes, biological variation resulting from recombination, mutation, and selection, population genetics, use of genetic methods to analyze protein function, gene regulation and inherited disease

    主題包括：基因、染色體與基因組的結構和功能；來自於基因重組、突變和篩選的生物變異；族群遺傳學；運用遺傳學的方法分析蛋白質的功能，基因的調控和遺傳性疾病。
  8. The cytogenetic tests deal with all chromosomal analysis for different diseases. the molecular tests investigate about 40 genetic diseases and the biochemical tests mainly investigate enzymes and proteins products of genetic diseases

    細胞染色體分析對不同疾病進行染色體分析，分子遺傳學檢驗對大約40種的遺傳疾病進行測試，而生化遺傳檢驗則主要檢驗病人體內酵素及蛋白質的含量，以測試有關的遺傳疾病。
  9. 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。
  10. 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 % 。
  11. Chromosome karyotypintg. the classical method in the technology of chromosome genetic analysis, is one of the important means in genetic research and supplementary clinical diagnosis. and it is then key index to analyze chromosome translocation or deficiency, and diagnosis of a variety of genetic diseases. the goal of chromosome analysis is to relate deviations from normal structure to biological or clinical effects

    染色體核型分析，染色體遺傳分析技術的經典方法，是遺傳學科學研究和輔助臨床診斷的重要手段之一，是分析染色體易位，缺失，診斷各種遺傳病變的關鍵指標，染色體分析的目的就是要確定細胞或個體的染色體組成，尤其是要將其與正常結構間的偏差和生理的或臨床疾病關聯起來。
  12. A better knowledge of their etiologic factors and their pathogenesis could have important practical implications for prevention. it is well known that maternal age is one of etiologic factors. but maternal age is just the effects of accumulated environmental factors on human body

    已有的研究發現母親生育年齡是染色體不分離疾病發生的危險因素，但母親生育年齡只是環境因子在體內累積作用的表現形式，隨著人們生活水平提高，人類生存環境發生了很大的變化，有必要分離當前與染色體不分離有關的環境因子，從而有利於預防染色體不分離疾病的發生，提高我國人口素質，降低人口數量。
  13. Linkage analysis plays an important role in gene mapping. the foundation : the two gene locuses which locate on the same chromosomal ( eg. disease gene and marker gene ) happen to cross over and recombine. the farther the distance between two locuses is, the higher the probability happening to cross over is, the lower the probability that the two locuses are inherited to offspring together is, that is, the degree of linkage is not strong. so we can estimate the distance and the degree of linkage by the recombination fraction between the two locuses to locate gene

    連鎖分析是基因定位主要策略之一，其基本原理是位於同一染色體上兩個基因位點（例致病基因與標記基因）在減數分裂的過程中會發生交換與重組，染色體上的兩個位點間距離越遠，發生重組的概率就越大，兩個位點在一起傳給後代的機會就越少，即連鎖程度弱，這樣由標記位點與疾病位點間的重組率可估算出兩者間的距離以及連鎖程度，達到基因定位的目的。
  14. 8p22 of human chromosome is an region rich in disease - related genes and is also the susceptible loci of oncogenes and tumor suppressor genes

    人染色體8p22區是一個富含疾病基因的區域，是癌基因和抑癌基因的研究熱點。
  15. Especially for the study of chinese y chromosome diversity, disease distribution, the origin of the nationality han, and flow disciplines, the distribution data and areas of the top 300 common chinese names would provide new clues and information which have the highest valuation in research and practical use

    尤其是中國人前300個常見姓氏的數據和分佈地區，對于研究中國人y染色體多樣性疾病的分佈漢民族源和流以及其他學科領域，都有可能提供新的線索和參考，具有極高的研究和實際使用的價值。
  16. From what you eat and drink to where you live, there ' s a special sickness lying in wait just for you if you have the misfortune to have two x chromosomes

    如果很不幸你的基因是由兩個x染色體組成，那麼從你吃喝的東西到你生活的地方，這兒都有個專門的疾病在靜靜地等待著你。
  17. This disease with autosomic recessive transmission, begins generally either in childhood, adolescence or young adulthood

    這種常染色體的退行性傳遞疾病，通常起病于孩童時期、青春期、或者成年人的早期。
  18. In addition, he has made significant contributions to the mapping and annotation of human chromosome 7, and, identification of many other disease genes

    除此以外，在斷定人類第七組染色體以及許多其他疾病基因，作出了重大的突破。
  19. Professor tsui is a discoverer of the gene for cystic fibrosis and has made significant contributions to the mapping and annotation of human chromosome 7 and identification of many other disease genes

    徐教授斷定了囊狀纖維的缺陷基因。此外，在鑒定人類第七組染色體及許多其他疾病基因亦作出了重大的突破。
  20. Chromosome disorders, one of the most important genetic diseases, are the most frenquent cause of mental retardation. these disorders are thus important public health problems for no entirely satisfactory prevention measures now exist

    染色體不分離所導致的疾病是最主要的遺傳病之一，也是導致智力發育障礙的最主要原因，其發生給社會和家庭帶來極大的負擔，其中以down綜合征（ ds ）最為常見。
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