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syndactyly相关的网络例句

查询词典 syndactyly

与 syndactyly 相关的网络例句 [注:此内容来源于网络,仅供参考]

Syndactyly is defined as simple when it involves soft tissue only or complex when it involves the bone or nail of the adjacent fingers or toes that are joined side by side.

简单的并指畸形定义只包括软组织,复合的定义包括连接临近手指或脚趾的骨或指甲。

Complex syndactyly refers to fingers joined by bone or cartilaginous union, usually in a side-to-side fashion at the distal phalanges.

复合并指畸形表明手指由骨或软骨连接,通常形成在指末端形成并排形式。

Fingerweb flap was frifted to treat 5 cases of congenital incomplete cutaneous syndactyly.

采用指蹼皮瓣滑移术治疗先天性不完全性皮肤性并指畸形5例。

Paper 1:Functional Analysis of the HOXD13 Mutants Associated with Syndactyly TypeⅤand SynpolydactylyIncidence of congenital limb malformation among the newborn population is 1‰-2‰.

论文一HOXD13基因p.Q317R突变和多聚丙氨酸延展突变的功能研究肢体畸形在新生儿中发生率为1‰-2‰,可单独出现也可作为综合征的一种表型。

In this study,we focused on the functional analysis of HOXD 13 p.Q317R mutant and polyalanine expansion mutant.PartⅠ:Functional Analysis of the HOXD13 p.Q317R Mutant Associated with Syndactyly TypeⅤHox gene encodes a family of transcription factors of fundamental importance for body patterning during embryonic development.

第一部分HOXD13同源盒p.Q317R点突变的功能分析同源盒基因(homeobox genes,Hox genes)编码一个高度保守的转录因子家族,在决定胚胎期细胞的定向分化与增殖以及调控机体组织器官的发育过程中起关键性作用。

Frifting fingerweb flap is an ideal solutions to treat congenital incomplete cutaneous syndactyly.

指蹼皮瓣滑移术是治疗先天性不完全性皮肤性并指畸形的理想方法之一。

Hand deformities ; congenital ; Syndactyly ; Classification ; Microsurgery

手畸形;先天性;并指;分类法;显微外科手术

Non-syndromic syndactyly is classified into five types according to Temtamy and McKusick.

HOXD13 N端多聚丙氨酸延展突变可以导致Ⅱ型并指,也称为并多指(synpolydactyly,SPD)(MIM 186000),主要临床表现为手部第3、4指并指,足部第4、5趾并趾,常伴蹼中全部或部分多指。

Result: in three categories and ten examples of congenital malformation fetus, the morphological and histological structures of colon in syndactyly and sxtrodactyly fetus have no obvious abnormity; the colon's structure shows abnormity in omphalo-thoracopagus twins; the colon's structure was insufficient development in anencephaly fetus.

结果:三类10例先天性畸形胎儿中,并缺指畸形胎儿结肠的形态学及组织学结构无明显异常;胸腹联体胎儿结肠结构异常;无脑儿结肠组织结构发育不全。

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