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Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation

机译：非思科智能迟滞的患者CDK5R1和OMG基因的编码区和UTR中的突变和新多态性

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Marco Venturin; Silvia Moncini; Valentina Villa; Silvia Russo; Maria Teresa Bonati; Lidia Larizza; Paola Riva;
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1. EDNRB基因编码区点突变及多态性在浙江地区散发性先天性巨结肠症中的检测与分析 [J] . 周妙妮, 李继承, 丁世萍分子细胞生物学报（英文版） . 2006,第001期
2. Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation. [J] . Venturin M, Moncini S, Villa V, Neurogenetics . 2006,第1期

机译：非综合征性智力低下患者CDK5R1和OMG基因编码区和UTR的突变和新型多态性。
3. Analysis of highly conserved regions of the 3'UTR of MECP2 gene in patients with clinical diagnosis of Rett syndrome and other disorders associated with mental retardation [J] . Mónica Santos, Jin Yan, Teresa Temudo, Disease Markers . 2008,第6期

机译：具有Rett综合征和其他与智障相关疾病的临床诊断的患者中MECP2基因3'UTR高度保守区域的分析
4. Analysis of highly conserved regions of the 3'UTR of MECP2 gene in patients with clinical diagnosis of Rett syndrome and other disorders associated with mental retardation [J] . Monica Santos, Jin Yan, Teresa Temudo Disease markers . 2008,第6期

机译：患有Rett综合征和其他与智力障碍相关疾病的临床诊断的患者中MECP2基因3'UTR高度保守区域的分析
5. MutationView: An Integrated Knowledge Base for Mutations and Polymorphisms in Human Disease Genes - Automatical Extraction of Disease-Associated Knowledge - [C] . Masafumi Ohtsubo, Susumu Mitsuyama, Takashi Kawamura, International Conference on Genome Informatics . 2003

机译：突变视图：人类疾病基因突变和多态性的综合知识基础 - 疾病相关知识的自动提取 -
6. K-ras andp53 mutations and DNA repair genes polymorphisms as biomarkers for lung cancer. [D] . Gao, Weimin. 2003

机译：K-ras和p53突变和DNA修复基因多态性作为肺癌的生物标记。
7. Analysis of Highly Conserved Regions of the 3’UTR of MECP2 Gene in Patients with Clinical Diagnosis of Rett Syndrome and Other Disorders Associated with Mental Retardation [O] . Mónica Santos, Jin Yan, Teresa Temudo, 2008

机译：Rett综合征和其他与智力障碍相关疾病的临床诊断患者中MECP2基因3UTR的高度保守区域分析
8. Analysis of Highly Conserved Regions of the 3'UTR of MECP2 Gene in Patients with Clinical Diagnosis of Rett Syndrome and Other Disorders Associated with Mental Retardation [O] . Santos M, Yan J, Temudo T, 2008

机译：Rett综合征和其他与智力障碍相关疾病的临床诊断患者中MECP2基因3'UTR高度保守区的分析

Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation

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