染色體遺傳 的英文怎麼說

中文拼音 [rǎnshǎitǐyízhuàn]
染色體遺傳 英文
chromosomal inheritance
  • 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。
  • 遺 : 遺動詞[書面語] （贈與） offer as a gift; make a present of sth : 遺之千金 present sb with a gener...
  • 傳 : 傳名詞1 （解釋經文的著作） commentaries on classics 2 （傳記） biography 3 （敘述歷史故事的作品）...
  • 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...
  • 遺傳 : [生物學] heredity; hereditary; inheritance; inherit
  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. However, only three species of the cephalochordate including b. lanceolatum, b. floridae, and b. belcheri, have so far been studied for their chromosome numbers, and the karyotypic analysis and banding study of amphioxus chromosomes remains largely untouched

    Floridae 、 b belcheri三種文昌魚染色體數目。有關文昌魚染色體核型和帶型的研究尚未見任何報道，文昌魚染色體核型和帶型的研究將為比較基因組學和細胞遺傳學研究提供珍貴的背景資料。
  3. Cytogenetic studies were made on several hybrid scallops using the karyotype method. hybridizations between chlamys farreri and patinopecten yessoensis, c. farreri and chlamys nobilis were studied

    本論文在染色體水平對蝦夷扇貝櫛孔扇貝雜交以及櫛孔扇貝華貴櫛孔扇貝正反交等幾個扇貝雜交組合進行了細胞遺傳學研究。
  4. The same phenomenon was observed in interspecific hybridization between chlamys farreri and chlamys nobilis. the karyotypes of adult hybrids and their parents were analyzed and compared. the chlamys nobilis ' s diploid chromosome number is 2n = 32, karyotype consists of 6m + 26t, nf = 38

    對該雜交組合的親本華貴櫛孔扇貝的染色體核型分析表明，華貴櫛孔扇貝雜交扇貝的細胞遺傳學研究共有zn = 32條染色體，核型公式為2n = 32 = 6m + 26t ，染色體臂數nf = 38 。
  5. 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。
  6. Episome is an additional genetic element that can exist either as an autonomous entity or be inserted into the continuity of the chromosome of a host cell.

    附加體是能插入寄生細胞連續的染色體之中，也能以自主實體而存在的一種附加遺傳因素。
  7. Twenty cases of euchromosome viewy genetic ill were analyzed in five years

    20例常染色體顯性遺傳病5年隨訪結果分析
  8. Consider as what recessive heredity causes euchromosome to high myopia

    對于高度近視則認為是常染色體隱性遺傳引起的。
  9. Former and scarce, for euchromosome dominance heredity, begin to last all one ' s life from the baby

    前者少見，為常染色體顯性遺傳，從嬰兒開始持續終生。
  10. Y chromosome is transmitted in the form of hap - loid, leading to extreme disequilibrium of y chromosome genetic markers distribution in different population. the prerequisite of str application in forensic medicine is establishment of a database of population y - str loci haplotype distribution. therefore we need to form haplotypes by using the known highly polymorphic str loci and detect more local population

    由於y染色體呈單倍體遺傳，導致y染色體遺傳標記在不同人群中的分佈極不平衡，群體差異比常染色體str位點更加顯著，在法醫學應用的前提條件是：建立含有多個y - str位點的單倍型的群體分佈數據庫。
  11. Chromosome theory of inheritance

    染色體遺傳學說
  12. Chromosome karyotyping, the classical method in the technology of chromosome genetic analysis, is one of the important means in genetic research and supplementary clinical diagnosis

    染色體核型分析，是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。
  13. 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。
  14. Facing to manufacturing system, this paper analyzed its characters and evolvement of production management modes, demonstrated that lean production and human - based theory were practical ways to reform our manufacturing systems fit for the reality. a division method was raised to separate the job - scheduling problem into shop and station types, and emphasis was pressed on the study of partheno - genetic algorithm ( pga ), a revised genetic algorithm, to calculate this problem. a new kind of gene joint - move algorithm was also raised

    針對製造系統，分析其生產管理模式的特點和變遷，論證了精益生產和以人為本的思想是適合現階段我國實際的製造系統管理模式改造途徑，對其中的主要具體問題?作業計劃調度提出shop （車間）和station （工作站）型兩分法，求解上重點研究了遺傳演算法的改進型式?單染色體遺傳演算法（ pga ）的基本理論，提出一種基因聯合移位運算元，證明了演算法的有效性與優越性，研究了如何將pga應用於製造系統作業調度這一復雜的組合優化問題，針對生產中總時間最短和jit兩種生產性能指標，給出了具體的解決方案及運算過程。
  15. Study on chromosome hereditary stability of the garlic tissues of dividing and growing when cultured

    大蒜分生組織培養的染色體遺傳穩定性研究
  16. The inheritance algorithm of a kind of chromosomes with changeable length to solve the bin - packing problem

    求解裝箱問題的一種變長度染色體遺傳演算法
  17. Y - str has many advantages over other genetic markers and it has become a hot topic of both application and research in forensic medicine

    與其他遺傳標記相比， y - str具有許多優點，正成為y染色體遺傳標記中法醫學應用和研究的熱點。
  18. In chapter four, first, the concept and basic flow of genetic algorithm is introduced, as well as a genetic algorithm based on variable length coding

    第四章：首先介紹了遺傳演算法概念及其基本流程，並對變長染色體遺傳演算法作了一個簡要介紹。
  19. Objective in order to improve the discrimination power and exclusion chance of polymorphic markers on chromosome y, it is necessary to cast about for novel y - str loci and to develop a new method to genotype y - snp for forensic science

    目的為了提高y染色體遺傳標記的個人識別能力和非父排除能力，尋找新的y - str和建立新一代遺傳標記y - snp的檢測方法十分必要。
  20. They were suitable for improving identification power of polymorphic markers on chromosome y. our approach of hplc can separate the oligonucleotides with different size and same size with different sequences, and provide a method to quantity products of snupe

    單倍型變異度表明這8個丫str具有較好的個人識別能力和非父排除率，能夠較好地提高y染色體遺傳標記的個人識別和非父排除能力。
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