1.
					
							Mutations in the ED1 Gene of X-linked Hypohidrotic Ectodermal Dysplasia;
						
					
					
						
						
					
					
						X性连锁少汗性外胚叶发育不良ED1基因的突变分析
					2.
					
							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
					3.
					
							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
					4.
					
							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。
					5.
					
							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
					6.
					
							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
					7.
					
							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
					8.
					
							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。
					9.
					
							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
					10.
					
							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
					11.
					
							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
					12.
					
							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
					13.
					
							Study on rapid diagnosis of spondyloepiphyseal dysplasia tarda family
						
					
					
						
						
					
					
						X连锁迟发性脊柱骨骺发育不良快速基因诊断方法的研究
					14.
					
							X-linked Inhibitor of Apoptosis Protein cDNA Transfection on Ovarian Carcinoma Cell Tolerance to Cisplatin
						
						
						X连锁凋亡抑制蛋白cDNA转染与卵巢癌细胞顺铂耐药性
					15.
					
							A novel mutation in the ALAS2 gene causes X-linked sideroblastic anemia.
						
					
					
						
						
					
					
						X连锁性铁粒幼细胞贫血家系新发现ALAS2基因G514A突变
					16.
					
							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
					17.
					
							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
					18.
					
							Protective Effect of X-linked Inhibitor of Apoptosis Protein (XIAP) in Hypoxic-ischemic Neonatal Mice Brain;
						
						
						X-染色体连锁的凋亡抑制剂(XIAP)对新生鼠缺氧缺血性脑损伤的保护作用