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- mandibular dysostosis and peromelia 下颌骨发育不全及四肢畸形
- There is something wrong with the mandibular joint. 你的下颌关节有点问题。
- The cysts are most often seen in the mandibular ramus or angle. 角化囊肿拥有明显的组织病理表徵，且以局部侵袭性和特高再发率著称。
- PR has especial diagnosis value for mandibular fractures. :PR优点是对下颌骨骨折诊断准确率高 ;
- Application of internal rigid fication in the mandibular fracture. 坚固内固定技术在下颌骨骨折中应用体会。
- The chin occupied 2/3 of the entire mandibular height. 上中下面高几乎各占全面高的1/3,上面高略大; 上唇与下颌高度比为1/2,下唇与下颌高度比略等于1/3,颏部与下颌高的比值略为2/3。
- The fistula was connected with mandibular body but the first molar. 颊瘘与外斜线相连,与下颌第一磨牙根尖不相通连。
- An Applied Anatomical study on the marginal mandibular Branch of facial nerve. 面神经下颌缘支的应用解剖学研究。
- Influence of inserting occlusal splints on the position of mandibular condyle. 咬合板高度对下颌髁突位置的影响。
- 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。
- The chin occupied more than 60 percent of the entire mandibular height. 颏占下颌高度的 60%25多。
- The SNB angle and mandibular plane angle (SN-MP) have no change (P>0.05). SNB及下颌平面角SN-MP无变化;P>0.;05;
- X-ray cephalometry showed some cases with light mandibular prognathism. 均为替牙期功能性反牙合，X线头影测量显示部分病例为轻度下颌前突。
- 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'?
- RE is partly or completely attached to the distal root of mandibular molars. 远舌根通常细短弯曲,它的出现增大了下颌第一磨牙根管治疗的难度。
- Mandibular overdenture with 2 magnetic attachment has more value in clinic. 2基牙磁性附着体制作下颌全口覆盖义齿具有良好的临床应用价值。
- 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。
- Methods: The model of mandibular defect was created in sixty Wistar rats. 方法：在60只大鼠一侧下颌骨体部形成下颌骨缺损模型，并随机分为3组，每组20只。
- 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'?
- 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'?
