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1)  developmental genetic models
发育遗传模型
2)  Genetic and breeding model
遗传育种模型
3)  developmental genetics
发育遗传
1.
Advance on the developmental genetics of quantity trait in crop;
作物数量性状发育遗传的研究进展
2.
unconditional model referred to the analysis of cumulative measurements along the developmental stages, and conditional model referred to the gain analysis throughout the developmental stages, were used to analyse the developmental genetics of valine content at different grain filling stages in the indica-japonica hybrid rice.
采用可以估算不同发育时期基因累加效应和特定发育时期净遗传效应的遗传模型和统计分析方法,研究了不同环境条件下籼粳交稻米灌浆过程中缬氨酸含量的发育遗传规律。
4)  genetic model
遗传模型
1.
Analysis on the genetic models for main characters in wheat;
小麦主要性状的遗传模型分析
2.
A genetic model was proposed for simultaneously analyzing genetic effects of nuclear,cytoplasm,and nu- clear-cytoplasmic interaction(NCI)as well as their genotype by environment(GE)interaction for quantitative traits of diploid plants.
提出了能分析二倍体植株数量性状核质互作效应的遗传模型,该模型把控制数量性状总的遗传效应分为核效应、质效应和核质互作效应,以及它们分别与环境作用的效应。
3.
Objective To explore the genetic model of systemic lupu s erythematosus(SLE).
结论 系统性红斑狼疮为加性遗传模型 ,基因频率为 0 。
5)  Inheritance model
遗传模型
1.
The near-isogenic lines of the rice cross Jing Diao 3(Japonica rice)× Towada(Indica rice) ,were need to studies the genetic the cold tolerance characters at the booting stage in their progeny family groups by utilizing the method of major gene plus polygene mixed inheritance model and joint analysis method of segregating plus non-segregating generations.
采用主基因+多基因混合遗传模型和分离世代加不分离世代联合分析的方法,对云南稻种粳掉3号与十和田构建的近等基因系(NILs)的衍生后代家系群体的孕穗期耐冷性状进行遗传研究。
2.
The method of major gene plus polygene mixed inheritance model was used to analyze the genetics of yield traits and fiber qualities in (Simian 3×TM1) and (Simian×CARMEN).
对(泗棉3号×TM 1)(组合Ⅰ)和(泗棉3号×CARMEN)(组合Ⅱ)的产量与品质性状进行遗传模型分析,得到有关产量与品质性状的最适遗传模型,其中组合Ⅰ子指的最适遗传模型为负向显性主基因+多基因模型,铃重最适遗传模型为等显性主基因+多基因混合遗传模型,衣分、单株铃数的最适遗传模型分别为两对主基因+多基因和一对主基因+多基因模型。
6)  Developmental genetics
发育遗传学
补充资料:Albright遗传性骨发育不全综合征


Albright遗传性骨发育不全综合征


因女性比男性为2∶1,支持伴X染色体显性遗性,为单一的突变基因引起。表现:身材矮小,最后身高137~152cm,偶尔正常,中等胖。圆脸,低鼻梁。出牙推迟,发育不全和/或■质发育不全。掌骨及骨短,尤其是第4及5,拇指末节短,圆锥形骨骺。皮下组织及基底神经节有钙化区。变化不定的低钙血症及高磷酸盐血症。青春期及妊娠期谨慎地应用维生素D治疗是需要的。智力不全,智商20~99。平均约60,偶尔有正常者。
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