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Constitutional 763.3 Kb chromosome 1q43 duplication encompassing only CHRM3 gene identified by next generation sequencing (NGS) in a child with intellectual disability

机译：宪法763.3 KB染色体1Q43重复包括在具有智力残疾的儿童中下一代测序（NGS）鉴定的CHRM3基因

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Xiaofei Cheng; Qifang Yang; Jun Liu; Juan Ye; Huiying Xiao; Gaimei Zhang; Yuanyuan Pan; Xia Li; Ruifeng Hao; Yinfeng Li;
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1. Constitutional 763.3 Kb chromosome 1q43 duplication encompassing only CHRM3 gene identified by next generation sequencing (NGS) in a child with intellectual disability [J] . Xiaofei Cheng, Qifang Yang, Jun Liu, Molecular cytogenetics . 2019,第1期

机译：宪法763.3 KB染色体1Q43重复包括在具有智力残疾的儿童中下一代测序（NGS）鉴定的CHRM3基因
2. Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability [J] . Sepideh Mehvari, Farzaneh Larti, Hao Hu, Molecular Genetics & Genomic Medicine . 2020,第10期

机译：全基因组测序识别包含智商残疾的大型伊朗家庭XQ13.2Q13.3的重复区域
3. Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1 [J] . Chih-Ping Chen, Hoi-Kin Yip, Liang-Kai Wang, Taiwanese journal of obstetrics and gynecology . 2017,第3期

机译：包含 ATRX 的产前检测到的1.484-Mb Xq13.3-q21.1重复的分子遗传学表征，以及Xq13重复的男性的综合征性智力障碍和先天性异常的文献综述。 3-q21.1
4. The Human Chromosomal Fragile Sites More Often Involved in Constitutional Deletions and Duplications - a Genetic and Statistical Assessment [C] . Dora Prata Gomes, Inês J. Sequeira, Carlos Figueiredo, International Conference of Computational Methods in Sciences and Engineering . 2016

机译：人类染色体脆弱的位点更常见于宪法缺失和重复性 - 遗传和统计评估
5. Using Next Generation Sequencing (NGS) to identify and predict microRNAs (miRNAs) potentially affecting Schizophrenia and Bipolar Disorder [D] . Williamson, Vernell Seay 2012

机译：使用下一代测序（NGS）识别和预测可能影响精神分裂症和双相情感障碍的microRNA（miRNA）
6. Constitutional 763.3 Kb chromosome 1q43 duplication encompassing only CHRM3 gene identified by next generation sequencing (NGS) in a child with intellectual disability [O] . Xiaofei Cheng, Qifang Yang, Jun Liu, 2019

机译：智力障碍儿童的宪法性763.3 Kb染色体1q43复制仅包含通过下一代测序（NGS）鉴定的CHRM3基因
7. Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1 [O] . Chih-Ping Chen, Hoi-Kin Yip, Liang-Kai Wang, 2017

机译：包含aTRX的产前检测到的1.484-mb Xq13.3-q21.1重复序列的分子遗传学特征以及在Xq13.3-q21.1重复的男性中的综合征智力残疾和先天性异常的文献综述

Constitutional 763.3 Kb chromosome 1q43 duplication encompassing only CHRM3 gene identified by next generation sequencing (NGS) in a child with intellectual disability

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