1.
Diagnosing X-linked Ichthyosis by Monoplast Single-round Duplex PCR
单细胞单轮二重PCR诊断X-连锁鱼鳞病
2.
Two main modes of inheritance exist: X-linked and autosomal dominant.
本病存在两种主要的遗传方式：X-连锁型和常染色体显性型。
3.
The inheritance pattern of EDMD includes X-linked recessive, autosomal dominant and recessive modes.
其遗传方式为X-连锁隐性、染色体显性和隐性遗传。
4.
X-linked Adrenoleukodystrophy: Metabolic Defect and Pharmacological Therapy;
X-连锁肾上腺脑白质营养不良发病机理及药物治疗的研究
5.
Molecular Biological Studies of X-linked Adrenoleukodystrophy;
X-连锁肾上腺脑白质营养不良的分子生物学研究
6.
Medical Research and Gene Detection in a Family with X-linked Liphoproliferative Disease;
X-连锁淋巴细胞异常增生症—家庭临床调查和基因检测
7.
Mutations of the SEDL Gene in X-linked Spondyloepiphyseal Dysplasia Tarda;
X-连锁迟发性脊椎骨骺发育不良SEDL基因突变研究
8.
Molecular Study of X-linked Spondyloepiphyseal Dysplasia Tarda in a Large Chinese Kindred;
X-连锁迟发性脊椎骨骺发育不良的分子遗传学研究
9.
Structure and Function of X-linked Adrenoleukodystrophy Protein
X-连锁肾上腺-脑白质营养不良蛋白的结构与功能
10.
Market Localization Research of X Chain Pharmarcy in Heilongjiang Province;
黑龙江省X连锁药店的市场定位研究
11.
Research Advances of the Relation between XIAP and Cancer
X连锁凋亡抑制蛋白XIAP肿瘤相关性研究现状
12.
Expression and significance of X-linked inhibitor of apoptosis protein in bladder cancer
X连锁凋亡抑制蛋白在膀胱癌的表达及其意义
13.
Skewed X Chromosome Inactivation and Imprinted/X-linked Gene Expression in Human Embryonic Stem Cells
人类胚胎干细胞X染色体倾斜性失活及印迹、X连锁基因表达状态
14.
Investigation on Genetic Linkage Analysis of X-linked Retinitis Pigmentosa Using Microsatellite Markers;
应用微卫星多态位点对X连锁型视网膜色素变性疾病进行遗传连锁分析的研究
15.
Genetic Linkage Localization and Mutation Analysis of Chinese X-linked Retinitis Pigmentosa Pedigrees;
我国X连锁型视网膜色素变性家系的基因连锁定位及突变的分析研究
16.
Detection of EDA Gene Mutation in a Pedigree of Han Nationality in Xinjiang with X-linked Hypohidrotic Ectodermal Dysplasia (XLHED);
一新疆汉族X连锁少汗性外胚叶发育不全（XLHED）家系EDA基因突变检测
17.
Clinical Study and Exclusive Genetic Mapping on X Chromosome in the X-linked Dominant Inherited Alport s Sydrome;
X连锁显性遗传性肾炎一家系临床及相关基因排除定位分析
18.
Mapping and Identified the Causative Genes in Chinese Nonsyndromic X-linked Hereditary Hearing Loss Pedigrees;
非综合征型X连锁显性遗传耳聋家系致病基因的定位及鉴定研究