genetic deficiency 中文意思是什麼
genetic deficiency
解釋
遺傳缺陷- genetic : adj. 1. 遺傳（學）上的。2. 發生的，發展的；創始的。adv. -ically
- deficiency : n. 1. 缺乏，不足，短缺。2. 缺陷。3. 不足額；虧空。
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This is due to genetic deficiency of the adrenocortical enzyme which normally converts that substrate to a nonandrogenic steroid in the biosynthesis of cortisol
這是由於在皮質醇生物合成中將底質轉變為非產生男性特徵類固醇的腎上腺皮質酶遺傳缺陷所致。 -
Dwarfism stunted growth. this may be due to genetic mutation, causing gibberellin deficiency
矮態：植物生長受到限制形成的植株形態矮小，可能是由於基因突變造成的赤霉素缺乏引起。 -
The mutant lines were crossed with deficiency lines on chromosome 2 and 3 respectively, and the genetic sites of 11 stocks have been determined. of them four showed a different phenotype from the known genes that control the heart development
分別將這些有心臟突變的品系與果蠅第二和第三染色體缺失系雜交，測定了11個品系的遺傳學位點，其中4個品系在遺傳學位點上有別于已經報道的心臟發育控制基因。 -
Other genetic disorders become apparent when the demands of an independent existence after birth reveal a disorder of function such as renal failure, increased susceptibility to infection, or mental deficiency
當出生后小兒獨立生存的需求呈現功能紊亂（如腎功能衰竭對感染敏感性增高或智力缺陷）時，另一些遺傳病就變為明顯。 -
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。 -
The researches acquired suggest that manipulating ferritin expression and other soluble components of seed iron in soybeans and possibly other seeds, using mendelian genetic technique and biotechnological approaches, could contribute to a sustainable solution to the global problem of iron deficiency
已有的研究表明，使用孟德爾遺傳方法和生物技術途徑提高大豆和其它穀物類種子中鐵蛋白的表達和其它可溶性鐵成分，將有助於全球性缺鐵問題的有效解決。 -
Primary carnitine deficiency is a genetic disease, which shows no apparent symptoms in either the parent or the infant. however, the affected child is threatened with the danger of sudden death before the age of one. cardiomyopathy may develop in their later childhood
有這種遺傳病的家庭父母一般都沒有明顯病徵，而患病的兒童可能在嬰兒時期（一般在一歲前）出現急性病徵，包括不省人事、低血醣，嚴重者會導致猝死。 -
A gene associated with primary carnitine deficiency, now called 0ctn2 was identified. mutations in 0ctn2 lead to this life - threatening disease. now, early genetic diagnosis of affected child is possible and appropriate treatments can be provided well in advance
此項發現能準確地確定患者的遺傳基因病變，及在患病家庭中分辨出攜帶基因者及患病者，從而可以及早進行適當的治療。
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