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- mutational dysostosis 突发性骨发育不全
- mutational dysostosis syndrome 突变性骨发育不全综合征, 赫尔克兰茨(氏)骨成形不全, 马-塞二氏综合征
- All sorts of mutational damage to animals' DNA would have occurred. 动物的脱氧核糖核酸可能遭到了各种各样的突变破坏。
- All sorts of mutational damage to animals'DNA would have occurred. 动物的脱氧核糖核酸可能遭到了各种各样的突变破坏。
- TP53 mutational status was compared with clinical outcome. 同时比较了TP53突变状况与临床结果的关系。
- Nelson H, Nelson N. title Cloning and mutational analysis of t ... 而在NCBI上的人体驱动蛋白马达域的 ...
- Objective To study the sensitivity and specificity of gene mutational analysis. 目的本文对脊肌萎缩症基因诊断的敏感性与特异性进行了研究。
- Objective: To investigate the echographic features and the value of fetal dysostosis by ultrasound. 目的探讨超声检查胎儿成骨发育不全的声像图特点及其诊断价值。
- These large populations facilitate the detection of rare mutational or recombinational events. 这样的大群体有利于检出稀有的突变或重组子。
- Nager syndrome (or acrofacial dysostosis) is an extremely rare congenital defect that has only had around 90 documented cases to date (02/06/07). 什么是'管理者综合征-罕见的先天性异常多系统综合征的面部特征'?
- Conclusion: Conventional ultrasound plays an important role in checking fetal dysostosis and is the first method in diagnosing the feta... 结论常规超声检查对胎儿成骨发育不全的筛检有着重要意义,为产前诊断胎儿骨骼发育异常的首选方法。
- Set an objectively scientific foundation for name, diagnosis, therapy and assessment of mutational falsetto. 目的 :为变声后“假声”的命名、诊断、治疗及疗效评价提供科学、客观的理论依据。
- Cleidocranial dysostosis or Cleidocranial dysplasia is a hereditary congenital abnormality of humans due to haploinsufficiency caused by mutations in the CBFA1 gene. 什么是'锁骨颅骨发育不全-罕见的遗传性疾病导致矮身材'?
- Doramectin, which is manufactured by mutational biosynthesis method, is a novel avermectin derivative. 道拉菌素是利用生物突变合成方法得到的新型阿维菌素族广谱抗寄生虫药。
- Treacher Collins syndrome (also known as Franceschetti-Zwahlen-Klein syndrome or mandibulofacial dysostosis) is a rare genetic disorder characterized by craniofacial deformities. 什麽是'特雷彻-柯林斯综合徵-遗传疾病造成面部和头颅畸形'?
- Objective To compare the effectiveness of heteroduplex, SSCP and heteroduplex-SSCP analyses in mutational screening. 目的比较异源双链、单链构像多态(SSCP)、异源双链-SSCP法筛查突变的效率，寻找简便有效的基因突变筛查方法。
- This article reports a 12-year-old boy suffered from cleidocranial dysostosis, the interim treatment progress, and considerations in treatment planning. 本篇报告将探讨锁骨颅骨成骨不全症之牙科临床症状表现，及治疗计画之考量。
- Mutational activation of the BRAF oncogene is the most common genetic alteration in cutaneous melanoma. BRAF癌基因突变的激活是皮肤黑色素瘤最常见的基因改变。
- Conclusion The PCR-SSP may be used for genotyping in mutational mononucleatide,and it has a good prospects. 结论PCR-SSP可对具有单核苷酸突变的基因分型,应用前景良好。
- Conclusion The PCR-SSP may be used for genotyping in mutational mononucleatide, and it has a good prospects. 结论PCR-SSP可对具有单核苷酸突变的基因分型，应用前景良好。
