Cryptic de novo deletion at 2q23.3-q24.1 in a patient with intellectual disability

HAMIDEH BAGHERIAN; JAMILEH MALBIN; MAHSA SHAFAEI; MOHAMMAD-SADEGH FALLAH; RAMIZ ALIEV; SIROUS ZAINALI2 5; TAHEREH POUR MOSTAFAEI; ZOHREH SHARIFI

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Cryptic de novo deletion at 2q23.3-q24.1 in a patient with intellectual disability

机译：智障患者在2q23.3-q24.1处进行从头开始的隐性删除

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《Journal of genetics》 |2016年第2期|共页
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HAMIDEH BAGHERIAN; JAMILEH MALBIN; MAHSA SHAFAEI; MOHAMMAD-SADEGH FALLAH; RAMIZ ALIEV; SIROUS ZAINALI2 5; TAHEREH POUR MOSTAFAEI; ZOHREH SHARIFI;
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中图分类遗传学;
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1. Cryptic de novo deletion at 2q23.3-q24.1 in a patient with intellectual disability [J] . Malbin Jamileh, Fallah Mohammad-Sadegh, Sharifi Zohreh, Journal of genetics . 2016,第2期

机译：智障患者在2q23.3-q24.1处进行从头开始的隐性删除
2. Identification of a patient with intellectual disability and de novo 3.7Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p15 [J] . HancarovaM., VejvalkovaS., TrkovaM., Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function . 2013,第1期

机译：鉴定智障患者和从头3.7Mb缺失支持2p14-p15中存在新型微缺失综合征
3. A new patient with a terminal de novo 2p25.3 deletion of 1.9?Mb associated with early-onset of obesity, intellectual disabilities and hyperkinetic disorder [J] . Maria Clara Bonaglia, Roberto Giorda, Sergio Zanini Molecular cytogenetics . 2014,第1期

机译：一名新患者，终末2p25.3缺失1.9？Mb，与肥胖，智力障碍和运动亢进的早期发作有关
4. Seizure detection using dynamic warping for patients with intellectual disability [C] . Lei Wang, Johan B. A. M. Arends, Xi Long, Annual International Conference of the IEEE Engineering in Medicine and Biology Society . 2016

机译：动态翘曲对智力障碍患者的癫痫发作检测
5. The Utility of Whole Exome Sequencing in Patients with Intellectual Disability and Developmental Delay as a First-Tier Diagnostic Testing Strategy [D] . ?Richardson, Ellen 2020

机译：全基因组测序的患者效用智障和发展迟缓的一线诊断测试策略
6. A new patient with a terminal de novo 2p25.3 deletion of 1.9 Mb associated with early-onset of obesity intellectual disabilities and hyperkinetic disorder [O] . Maria Clara Bonaglia, Roberto Giorda, Sergio Zanini 2014

机译：一名新患者的终末2p25.3缺失1.9 Mb与肥胖智力障碍和运动亢进的早期发作有关
7. Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene [O] . C. Bonnet, M.-J. Grégoire, M. Vibert, 2008

机译：患者在患者中缺少具有明显平衡的de Novo互易易位T（Q21; p23）的患者缺失与肌瘤 - 加综合征相关的患者：epsilon-sarcoglycan（sgce）基因的父母缺失

Cryptic de novo deletion at 2q23.3-q24.1 in a patient with intellectual disability

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