同种生物的个体对某些形态、形质等所表现的多样性的状态。
BACKGROUNDS This article aims to study the relationship between the polyalanine tracts expansion or polymorphism in exon 1 and point mutation in exon 2 of H0XA13 gene and Mullerian duct abnormalities.
背景本文主要研究了HOXA13基因多聚丙氨酸束长度改变或多态现象及同源结构域突变与苗勒管发育异常的关系。
参考来源 - 苗勒管发育异常患者HOXA13基因的研究·2,447,543篇论文数据，部分数据来源于NoteExpress
由共同多态现象确定的线粒体单倍群与疾病的危险因素和生存率相关。
Mitochondrial haplogroups defined by common polymorphisms have been associated with risk of disease and longevity.
人类基因组遗传多态现象研究的深入，导致了法科学领域个体识别和亲权鉴定发生根本性变化。
With the study advances on DNA polymorphism of human genome, radical changes have been taking place in forensic individual identification and paternity tests.
亚甲基四氢叶酸还原酶基因突变导致的遗传多态现象可增加神经管缺陷(ntd)发生的危险性。
The genetic polymorphisms due to mutations in the methylene tetrahydrofolate reductase gene may increase the risk for NTDs.
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