QTL等位基因变异与孟德尔基因变异具有类似的分子基础，即基因表达或蛋白质功能发生改变。
The allelic variations at QTL has similar molecular basis to the variations at simple Mendelian loci and the basis is that gene expressions or protein functions vary.
氟烷基因的遗传与孟德尔的分离定律是一致的。
The inheritance of the halothane gene was shown to be in agreement with Mendel's law of segregation.
我们在学校所教的“显性和隐形基因严格遵循孟德尔法则”的模型已被证明是比牛顿定律更简单的对事实的描述。
The models we were taught in school about "dominant" and "recessive" genes steering a strictly Mendelian process have turned out to be an even greater simplification of reality than Newton's laws.
孟德尔和他褶皱、光滑的豌豆很好的介绍了基因遗传，但是随后我们就会有种想法认为基因要不全能、要不不能影响二元性状。
Mendel and his wrinkly and smooth peas make a nice introduction to genetic transmission, but the downside is that we go away with the idea that genes have an all-or-nothing effect on a binary trait.
孟德尔式的基因并不是真正的实体，而是抽象概念或者是说明性的符号。
Mendelian gene is not a real physical entity but an abstraction or symbol.
通常上，孟德尔疾病的遗传诊断主要依靠临床诊断以及随后对疾病已知相关基因的测序。
Traditionally, the genetic diagnosis of a mendelian disorder relied on the establishment of a clinical diagnosis followed by the sequencing of previously implicated genes.
孟德尔的著作解释说，特性的遗传问题可以用代代相传的因子说明，这就是基因。
Mendel's work explained the inheritance of traits can be stated by factors passed from one generation to the next: a gene.
T1和T2代中潮霉素抗性表现为显性单基因位点的遗传方式，符合孟德尔分离规律，并得到分子鉴定结果的证实。
Mendelian inheritance of hygromycin resistance was showed as single dominant locus and proved by Southern blotting analysis in T1 and T2 generation of all transgenic plants.
家系调查表明这一位点的等位基因按孟德尔规律遗传。
The investigation results of familial members showed that this genetic marker system was in line with Mendelian's law.
根据孟德尔自由分离规律，从子代的基因型推断出亲代可能的基因。
And the genotypes of the parental oysters were assessed according to the Mendelian laws.
更重要的，16名患者(5.3%)有一个可以引起孟德尔疾病的基因组。
More importantly, 16 patients (5.3% of population) had a genomic profile likely to cause a Mendelian disorder.
结论外源基因(人组织蛋白酶k基因)已经整合到小鼠的染色体上，并且按孟德尔遗传定律中的分离定律进行遗传。
Conclusion the foreign gene (human Cathepsin K gene) has already integrated into mouse chromosome, and it can inherit in accordance with Mendelian inheritance.
基于综合的胚胎基因组，研究人员有效地进行了全基因组的孟德尔疾病诊断与人类白细胞抗原匹配试验。
Based on the comprehensive embryonic genome, we effectively performed whole-genome Mendelian disorder diagnosis and human leukocyte antigen matching tests.
基于综合的胚胎基因组，研究人员有效地进行了全基因组的孟德尔疾病诊断与人类白细胞抗原匹配试验。
Based on the comprehensive embryonic genome, we effectively performed whole-genome Mendelian disorder diagnosis and human leukocyte antigen matching tests.
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