ectodermal的例句大全

Clinical and genetic features of ectrodactyly, ectodermal dysplasia and clefting syndrome congenital absence of fingers and/ or toes.

先天性缺指（趾）-外胚叶发育不全-唇/腭裂综合征的临床和遗传学特点先天缺少手指或脚趾。

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The fore-gut and hind-gut are of ectodermal origin and the mid-gut arises from endoderm.

前肠与后肠起源于外胚层，中肠则发生自内胚层。

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Prenatal diagnosis of X-linked anhidrotic ectodermal dysplasia with X-chromosome inversion

X染色体倒位伴X连锁无汗性外胚叶发育不良一个家系的产前诊断

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a mutation in the connexin 30 gene in a pedigree with hidrotic ectodermal dysplasia

有汗性外胚层发育不良一家系的连接蛋白30基因突变检测

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objective: to study the complete dentures for children with hypohidrotic ectodermal dysphasia.

目的：研究少汗型外胚叶发育不良儿童的全口义齿修复。

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a family with anhidrotic ectodermal dysplasia ( aed) is reported. there were 8 male and 6 female patients in the family, and the male to female ratio was approximately 1 ∶ 1 and the condition belonged to autosomal dominant inheritance.

报道了无汗性外胚叶发育不全（EDA）一家系，患者既有男性，又有女性，男女比例接近1∶1，属常染色体显性遗传。

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Objetive : To detect the gene mutation of a patient with anhidrotic ectodermal dysplasia.

目的: 检测无汗性外胚层发育不全患者的EDA基因 的突变.

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Objective : To detect ED 1 gene mutation in three hypohidrotic ectodermal dysplasia ( HED ) nuclear families.

目的: 研究少汗性外胚叶发育不全引起先天缺牙的ED1基因突变.

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Objective To analyze genetic types and clinical features with anhidrotic ectodermal dysplasia ( EDA ).

目的分析无汗性外胚叶发育不全的遗传类型和临床特点.

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Ectodermal dysplasia showing clinical overlap between AEC, Rapp-Hodgkin and CHAND syndromes

外胚层发育不良症临床症状表现为AEC、Rapp-Hodgkin和CHAND综合征

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Gene Mutation Analysis in Chinese Patients with Ectodermal Dysplasia

外胚层发育不良的基因突变研究

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A Pedigree Study on Congenital Hidrotic Ectodermal Dysplasia

一个先天性有汗性外胚层发育不良家系的调查研究

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Oral rehabilitation nursing for patients with congenital ectodermal dysplasia

先天性外胚叶发育不全的口腔修复护理

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Congenital hidrotic ectodermal dysplasia: clinical and genetic features

有汗性外胚层发育不良临床及遗传特点分析

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Prognostic factors of primitive neuroectodermal tumor Research progress in the genes and proteins of hypohidrosis ectodermal dysplasia

原始神经外胚层肿瘤化疗患者预后的研究少汗型外胚层发育不良症相关基因及其蛋白

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The Clinical Analysis of A Large Rare Mongolian Family with Ectodermal Dysplasia

蒙古族罕见的外胚层发育不全症的临床分析

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