abnormality 专八

Such abnormalities can be prevented.

这类不正常现以预防的。

A routine scan revealed abnormalities in the fetus.

一次常规扫描发现胎儿畸形。

Male-sterility mainly results from the abnormality of mesospore,tapetum tissue and vascular bundle.

中层组织、绒毡层组织及药隔维管束异常均雄性败育的因素。

Objective To discuss the manifestations of neuropsychic disturbance and neuroprotenial abnormality resulted from acute arsenic poisoning.

目的探讨急性砷中毒致神经精神障碍神经电生理异常的临床表现,提高急性砷中毒在临床工作中的认识。

petit mal seizure accompanied by other abnormalities (atonia or automatisms or vasomotor changes).

癫痫小发作伴随着其他不正常的现。

Methods :Using the chromo somal analysis and flurospectrop hotomytry methods to expel the chromosomal abnormality and mucoplysacch aridosis.

方法染色体检查排除染色体病,采度计检测。

Cleidocranial dysostosis or Cleidocranial dysplasia is a hereditary congenital abnormality of humans due to haploinsufficiency caused by mutations in the CBFA1 gene.

什么'锁骨颅骨发育不全-罕见的遗传性疾病导致矮身材'?

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响，采小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的致突变性。

Even our sins are “revelational, that is, in their very abnormality.” (NS, 275.

就算我们的罪也具启示性，因为罪「反常」的。(NS,275.

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN突变引起血管的疾病，但没有认知的异常，这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中的作。

ECG-gated MRI was performed at 0.5T in 12 patients, aged from 2 months old to 10 years old, for assessment of complex congenital cardiac abnormalities of the asplenia syndrome.

摘要本研究运0.5T磁振造影来评估12个由年龄介于2个月至10岁间有无脾症候群患者先天性心脏病之关系。

Choanal atresia is often related to the presence of a congenital abnormality and only a few cases involve the occurrence of mucosal fibrosis of the surrounding choana after trauma.

摘要后鼻孔闭锁大多数先天性发育畸形有关，少部分因放射治疗导致后鼻孔周围黏膜组织伤害引起纤维化形成。

The research showed that the pollen of seedless wampee is approximately round in shape and unequigranular,It has a high abnormality rate,a low pollen germination rate and short pollen tubes.

对郁南无核黄皮花、果生长发育的生物学特性进行系统观察的结果表明:无核黄皮的花粉比有核黄皮的花粉略大,且大小不均匀,畸形率相对较高,花粉萌发率低,花粉管短;

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症一种罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。