1)X-linkedX连锁
1.Investigation on genetic linkage analysis of a family with X-linked retinitis pigmentosa;一个疑似X连锁型视网膜色素变性家系的遗传连锁分析的研究
2.Haplotype analysis of two families with X-linked retinitis pigmentosa;两例疑为X连锁型视网膜色素变性家系的单倍型分析研究
英文短句/例句
1.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
2.Research Advances of the Relation between XIAP and CancerX连锁凋亡抑制蛋白XIAP肿瘤相关性研究现状
3.Expression and significance of X-linked inhibitor of apoptosis protein in bladder cancerX连锁凋亡抑制蛋白在膀胱癌的表达及其意义
4.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
5.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
6.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
7.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
8.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
9.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
10.Identification and Characterization of the Gene Responsible for a Novel X-Linked Mental Retardation Syndrome一种新的X连锁精神发育迟滞综合征的致病基因克隆和功能分析
11.Study on rapid diagnosis of spondyloepiphyseal dysplasia tarda familyX连锁迟发性脊柱骨骺发育不良快速基因诊断方法的研究
12.Clinical and genetic analysis of 10 cases with X-linked agammaglobulinemia10例X连锁无丙种球蛋白血症的临床分析和基因诊断
13.X-linked Inhibitor of Apoptosis Protein cDNA Transfection on Ovarian Carcinoma Cell Tolerance to CisplatinX连锁凋亡抑制蛋白cDNA转染与卵巢癌细胞顺铂耐药性
14.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
15.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
16.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。
17.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。
18.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
相关短句/例句
XLRPX连锁RP
3)X-linkedX-连锁
1.Clinical features of 17 cases of X-linked agammaglobulinemia;17例X-连锁无丙种球蛋白血症临床表型分析
2.A report of two cases of severe X-linked combined immunodeficiency in one family and literature review;X-连锁严重联合免疫缺陷病一家系分析并文献复习
3.Related genes study on X-linked retinitis pigmentosa;X-连锁遗传视网膜色素变性相关基因研究概况
4)X-linked ALDX-连锁ALD
5)X-linkedX性连锁
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
6)X-linked inheritanceX连锁遗传
延伸阅读
X伴性连锁显性遗传X伴性连锁显性遗传X?linked do?minant inheritanec 病理基因位于X染色体上，现其性质显性的，这种疾病称X连锁显性遗传病。特点：①系谱中可看到连续传递。②男性患者的后代中，女儿都患病，儿子都正常；女性患者的后代中，则子女各有1/2可能患病。③一般女性患者为多。④患者的双亲中，有一方也是该病患者。
