缺失综合征,deletion syndrome
1)deletion syndrome缺失综合征
1.Progresses on the genetic study of 22q11deletion syndrome22号染色体长臂近端微片段缺失综合征的遗传学研究
英文短句/例句
1.Analysis of the clinical phenotype and pathogenesis in seven children with 22q11.2 deletion syndrome.22q11.2微缺失综合征7例相关临床表型及病因分析
2.Establishment and Application of Genetic Diagnostic System for Eight Chromosome Microdeletion Syndromes by Fluorescence in Situ Hybridization;8种微缺失综合征荧光原位杂交诊断体系的建立与应用
3.Study on Screening, Diagnosis and Intellectual Development Status in Children with Chromosome 22q11 Deletion Syndrome染色体22q11微缺失综合征的筛查与诊断及其智能发育状况的研究
4.Progresses on the genetic study of 22q11 deletion syndrome22号染色体长臂近端微片段缺失综合征的遗传学研究
5.Detection of Y chromosome microdeletions in azoospermic patients with Klinefelter′s syndromeKlinefelter综合征Y染色体微缺失的检测
6.acquired immunity deficiency syndrome获得性免疫缺乏综合征
7.sideropenic dysphagia syndrome缺铁性吞咽困难综合征
8.secondary antibody deficiency syndrome继发性抗体缺乏综合征
9.acquired immunodeficiency syndrome, AIDS获得性免疫缺陷综合征
10.Kallman syndrome性幼稚－失嗅综合征
11.Deletion of p15 Gene and Promoter Methylation in Myelodysplastic Syndromes骨髓增生异常综合征p15基因的表达缺失和启动子甲基化
12.Deletion of the p15 Gene and Promoter Methylation in the Bone Marrow of patients with Myelodysplastic Syndromes骨髓增生异常综合征患者骨髓p15基因的表达缺失与启动子甲基化
13.Establishment of RT-PCR for detection of nsp2 deletion porcine reproductive and respiratory syndrome virus猪繁殖与呼吸综合征病毒nsp2基因缺失株RT-PCR检测方法的建立
14.Muscle segment homeobox gene-1 and non-syndromic hypodontia同源异型盒基因-1与非综合征型多数牙先天性缺失
15.On College Student s Network Honest Lost and It s Comprehensive Treatment;浅谈大学生网络诚信缺失及综合治理
16.Sequence Analysis of the Deletion Region in PIS Goats and LINEs in Pig and Bovine Genome无角山羊间性综合征缺失片段及猪牛基因组中长散布元件的序列分析
17.Research on Angiotensin-converting Enzyme (Insert/Deletion) Gene Polymorphism in Children with Primary Nephrotic Syndrome血管紧张素转换酶基因插入/缺失多态性与儿童原发性肾病综合征的相关研究
18.Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation-dependent probe amplification多重连接探针扩增技术在先天性心脏病22q11微缺失/微重复综合征诊断中的应用
相关短句/例句
5p deletion syndromes5p缺失综合征
1.The term "5p deletion syndromes" is proposed to encompass all the patients.通过对丹麦Niebuhr实验室所提供的106例5p缺失患者临床诊断资料和染色体分析资料的研究，首先定义了“5p缺失综合征”。
3)Chromosome 22q11 deletion syndrome22q11微缺失综合征
4)22q11DS22q11缺失综合征(22q11DS)
5)22q11.2 deletion syndrome22q11.2微缺失综合征
1.Analysis of the clinical phenotype and pathogenesis in seven children with22q11.2 deletion syndrome.22q11.2微缺失综合征7例相关临床表型及病因分析
6)Xp21 contiguous gene deletion syndromeXp21邻近基因缺失综合征
1.Gene deletion analysis in a boy withXp21 contiguous gene deletion syndrome;Xp21邻近基因缺失综合征1例及其基因缺失分析
延伸阅读
缺失分子式：CAS号：性质：由于在核分裂中染色体DNA的某部分失落而引起的染色体变异。在某些情况下，在减数分裂的前期即可辨认出缺失，因为有一个环形（loop）生成，以使缺失区的两边都能进行正常的配对。
