1.
COL1A1 gene mutation in a family with osteogenesis imperfecta type Ⅳ
成骨不全症Ⅳ型家系COL1A1基因突变
2.
Genetic Studies of Osteogenesis Imperfecta Type Ⅰ and Two Candidate Genes of Osteoporosis;
Ⅰ型成骨不全及骨质疏松症两个候选基因的遗传学研究
3.
"hypochondroplAsia, similar except for normal head size;"
软骨发育不良,症状与软骨发育不全相似,但头部大小正常;
4.
The X-ray Performance of the Skeleton Change in Turner Syndrome Patients
先天性卵巢发育不全症骨骼改变的X线表现
5.
Improper development of cartilage at the ends of the long bones, resulting in a form of congenital dwarfism.
软骨发育不全在骨头尾部的软骨的不正常发育，从而引起先天性侏儒症
6.
Establishment of a finite element model:Canine segmental mandibular reconstruction by partial-cortical-cutting distraction osteogenesis
不完全截骨牵张成骨重建犬下颌骨节段缺失的有限元模型建立
7.
"Hereditary dwarfisms include achondroplAsia, with normal trunk size But short limbs and a large head;"
遗传性侏儒症包括︰软骨发育不全,躯干发育正常,但肢体极短,头较大;
8.
polyostotic fibrous dysplasia
多骨纤维性结构不良症
9.
"Severe combined immunodeficiency (SCID), which arises from several different genetic defects, disrupts all of these."
严重复合免疫不全症是由几个不同的遗传缺陷造成,因而全面瓦解。
10.
Sutural Distraction Osteogenesis (SDO) for Correction of Midface Hypoplasia: Experimental and Clinical Studies
缝牵引成骨矫正面中部骨骼发育不全的基础和临床研究
11.
A novel collagen,type Ⅰ,alpha Ⅰ mutation in a Chinese osteogenesis imperfecta family
成骨不全一家系1型胶原α1链基因新突变
12.
Tibetan Bone Bao Security Evaluation and Primary Pharmacological Study to Fracture and Osteoporosis
藏骨葆安全性评价及防治骨折与骨质疏松症的主要药效学研究
13.
HRMRI in assessment of trabecular bone micro-architecture in osteoporosis
高分辨率磁共振成像评价骨质疏松症骨微结构
14.
female gonadal dysgenesis
女性生殖腺发育不全症
15.
congenital ovarian agenesis
先天性卵巢发育不全症
16.
pituitary adiposity
垂体机能不全性肥胖症
17.
Genetic counselling and the management of complications in achondroplasia are important.
对于软骨发育不全侏儒患者的遗传谘询以及其并发症的处理是很重要的。
18.
A complete fracture is when the bone comes apart.
完全骨折是指骨头分成了好几块。