A Chromosome Breakpoint Mapping Strategy to Identify Candidate Genes for Nonsyndromic X-linked Mental Retardation within Xp11.2

Andreas Schroer; Catherine Bovie; Hans-Hilger Ropers; Ilke Slosarek; James Cox; Lucy Raymond; Sabine Kuebart; Simon Holden; Vera Kalscheuer

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A Chromosome Breakpoint Mapping Strategy to Identify Candidate Genes for Nonsyndromic X-linked Mental Retardation within Xp11.2

机译：染色体断点映射策略，以识别Xp11.2内非综合征X连锁精神发育迟缓的候选基因

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《Clinical Science》 |2003年第s49期|共页
作者
Andreas Schroer; Catherine Bovie; Hans-Hilger Ropers; Ilke Slosarek; James Cox; Lucy Raymond; Sabine Kuebart; Simon Holden; Vera Kalscheuer;
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中图分类临床医学;
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1. Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. [J] . Chen W, Jensen LR, Gecz J, European journal of human genetics: EJHG . 2007,第3期

机译：对464例非综合征性X连锁智力低下患者脑表达的X染色体miRNA基因进行突变筛选。
2. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint. [J] . De Baere-E, Van Roy-N, Speleman F, Genomics . 1999,第1期

机译：在3q23上关闭BPES基因：在45 kb粘粒中绘制de novo易位t（3; 4）（q23; p15.2）断点的图谱，并绘制三个候选基因RBP1，RBP2和beta'的图谱-COP，位于断点的远端。
3. Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes. [J] . Wirth J, Nothwang HG, van der-Maarel-S, Journal of Medical Genetics . 1999,第4期

机译：通过FISH对疾病相关的平衡染色体重排进行系统表征：通过细胞遗传学和基因锚定的YAC可以识别微缺失和智力低下基因的候选区域。
4. Initial study of candidate genes on chromosome two for relative hand skill [C] . C. Phillips, A. Barbara, M.V. Lareu, International Society for Forensic Genetics . 2006

机译：染色体两种候选基因的初步研究
5. Genetic linkage mapping in X-linked mental retardation not caused by fragile X [D] . Lazzarini, Alice Mary 1996

机译：X连锁性智力低下的遗传连锁映射不是由脆弱的X引起的
6. Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes [O] . J Wirth, H Nothwang, S van der Maarel, 1999

机译：通过FISH对疾病相关的平衡染色体重排进行系统表征：通过细胞遗传学和遗传锚定的YAC可以识别微缺失和智力低下基因的候选区域
7. Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation [O] . Chen, W., Jensen, L., Gecz, J., 2007

机译：464例非综合征性X连锁精神发育迟滞患者脑表达X染色体miRNa基因突变筛查

A Chromosome Breakpoint Mapping Strategy to Identify Candidate Genes for Nonsyndromic X-linked Mental Retardation within Xp11.2

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