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hypoplasia造句

1. Another lasting symptom commonly is enamel hypoplasia.
另一个持久的症状通常是牙釉质发育不全。

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2. The purpose is to increase the corpus callosum hypoplasia CT performance.
目的旨在提高对胼胝体发育不全ct表现的认识。

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3. The blunt ending of the cord is due to hypoplasia of the distal spinal cord.
脊髓末端圆钝是由于末梢脊髓发育不良。

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4. Objective To investigate the clinical character of congenital pulmonary hypoplasia.
目的探讨先天性肺发育不全的临床特征。

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5. Congenital abnormalities - cerebellar hypoplasia, ocular defects, weak small calves.
先天性畸形——小脑发育不全,眼缺陷,牛犊弱小。

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6. The anterior pituitary may be affected by absence or hypoplasia of the infundibulum.
垂体前叶可以受累而缺失或漏斗发育不良。

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7. Objective:To evaluate the sonographic features of hypoplasia of the right liver Lobe.
目的:探讨右肝发育不良的声像图特点。

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8. The amplification of skull base by changing skull′s form decreased hypoplasia of mid-face.
颅缝早闭症一定要扩大颅底才能彻底改变颅骨外形,减少以后中面部发育不良。

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9. As is implied by the name the most characteristic lesion is hypoplasia of the nasal turbinates.
顾名思义,最特征的病变是鼻甲发育不全。

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10. As is implied by the name, the most characteristic lesion is hypoplasia of the nasal turbinates.
顾名思义,最特征的病变是鼻甲发育不全。

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11. Objective: To investigate the value of diagnostic imaging for isolated right ventricular hypoplasia.
目的:探讨影像技术对孤立性右心室发育不全的诊断价值。

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12. GLUF has also been shown in mouse embryos to cause growth retardation increased death or hypoplasia.
研究表明,草安磷也造成小鼠胚胎发育迟缓、增加死亡或者发育不全。

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13. Purpose: To assess the diagnostic value of MRI and CAG in isolated right ventricular hypoplasia (IRVH).
目的:评价MRI诊断孤立右心室发育不全(IRVH)的价值,并与心血管造影(CAG)对比研究。

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14. Results The cause of congenital pulmonary hypoplasia may be related with heredity and virus infection early on fetus.
结果先天性肺发育不全的原因可能与遗传、胚胎早期病毒感染等因素有关。

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15. This child died soon after premature birth at 23 weeks gestation from pulmonary hypoplasia as a result of oligohydramnios.
婴儿因羊水过少导致的肺发育不良在孕23周早产后死亡。

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16. Conclusion there are the phenomena of hypoplasia in the gastrocnemius mep of the neonatal mouses with spina bifid a manifesta.
结论显性脊柱裂仔鼠腓肠肌运动终板有发育不全现象。

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17. Results: The trisomy with cleft palate mouse foetuses had significantly developmental hypoplasia in the primary palatal shelves.
结果:该模型虽无原发腭裂却伴有原发腭的发育不足;

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18. The pathogenesis of them: in 3 cases were muscle fiber structure hypoplasia, 3 cases were arteriosclerosis and 1case was arteritis.
病因有肌纤维结构发育不良3例、动脉粥样硬化3例、大动脉炎1例。

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19. The heart function of Scimitar syndrome should be followed-up for a long time for it usually associated with right lung hypoplasia.
但弯刀综合征多伴右肺发育不良,心功能情况还须长期随访。

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20. Objective:To explore the value of bone marrow biopsy in diagnosing Myelodysplastic Syndrome(MDS) especially in the cases of MDS with hypoplasia.
目的:评估骨髓活检在骨髓增生异常综合征尤其是低增生型病例时的诊断价值。

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21. Objective: to investigate the stability of internal midface distraction in correction of severe maxillary hypoplasia secondary to cleft lip and palate.
目的:初步研究和评价内置式牵引器牵引成骨治疗上颌发育不全术后的稳定性。

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22. Under light and electron microscope, it was seen that HCY 2 gene resulted in structure disturbance, endocardial cushion defect and hypoplasia of heart.
HCY2基因可引起心脏结构紊乱、心内膜垫缺损和抑制心室心房发育,并可损害心肌细胞的超微结构。

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23. METHODS: 3 children with hypoplasia of teeth were examined and analyzed carefully by clinical examination and laboratory test to find the genetic factors.
方法:采用临床、实验室检查方法对3例患儿进行详细的体检,并分析导致出现牙根发育不良表型的遗传学因素。

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24. It is a heterogeneous condition defined loosely by any combination of optic nerve hypoplasia, pituitary hypoplasia, and midline neuroradiological malformations.
它是一种异质性条件界定的任何视神经发育不全,垂体发育不良,畸形和中线影像学结合松散。

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25. This disease should be differentiated from variation of the large cisterna magna arachnoid cyst of the posterior forssa cystic neoplasm and severe hypoplasia of the cerebellum.
本病需与后颅窝蛛网膜囊肿、囊性新生物和变异的巨大枕大池以及重度小脑发育不全鉴别。

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26. Hypoplasia or absence of the major telencephalic commissures and a hypoplasia of corticospinal tracts to half the normal size, were the major neurodevelopmental defects we observed.
我们观察到的主要神经发育缺陷是发育不全、或者缺失主要的端脑连合处、皮质脊髓束因发育不全只有正常大小的一半。

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27. Hypoplasia or absence of the major telencephalic commissures and a hypoplasia of corticospinal tracts to half the normal size, were the major neurodevelopmental defects we observed.
我们观察到的主要神经发育缺陷是发育不全、或者缺失主要的端脑连合处、皮质脊髓束因发育不全只有正常大小的一半。

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