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A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach

机译：使用染色体微阵列分析方法检测到与7q和18p从头微缺失，Xp上的微复制和18q部分三体性相关的非综合征性智力障碍

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Irene Pinto; Lysa Minasi; Alex da Cruz; Aldaires de Melo; Damiana da Cruz e Cunha; Rodrigo Pereira; Cristiano Ribeiro; Claudio da Silva; Daniela de Melo e Silva; Aparecido da Cruz;
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1. A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach [J] . Irene Plaza Pinto, Lysa Bernardes Minasi, Alex Silva da Cruz, Molecular cytogenetics . 2014,第1期

机译：使用染色体微阵列分析方法检测到与7q和18p的从头微缺失，Xp的微复制和18q的部分三体性相关的非综合征性智力障碍
2. A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach [J] . Irene Plaza Pinto, Lysa Bernardes Minasi, Alex Silva da Cruz, Molecular cytogenetics . 2014,第1期

机译：使用染色体微阵列分析方法检测到与7q和18p的从头微缺失，Xp的微复制和18q的部分三体性相关的非综合征性智力障碍
3. Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication [J] . Yapijakis Christos, Angelopoulou Antonia, Manolakos Emmanuel, Advances in Experimental Medicine and Biology . 2020,第1期

机译：患有DE Novo 18Q微缺失和18P微杂质的患者中的颅面和神经表型
4. A Partial least squares-based regression approach for analysis of frontotemporal dementia gene markers in human brain gene microarray data [C] . S. C. Chan, H. C. Wu, J. Q. Lin, 2018 IEEE 23rd International Conference on Digital Signal Processing . 2018

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5. Classical and Bayesian mixed model analysis of microarray data for detecting gene expression and DNA differences [D] . Demirkale, Cumhur Yusuf. 2009

机译：芯片数据的经典和贝叶斯混合模型分析，用于检测基因表达和DNA差异
6. A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p microduplication at Xp and 18q partial trisomy detected using chromosomal microarray analysis approach [O] . Irene Plaza Pinto, Lysa Bernardes Minasi, Alex Silva da Cruz, 2014

机译：使用染色体微阵列分析方法检测到与7q和18p从头微缺失Xp上的微复制和18q部分三体性相关的非综合征性智力障碍
7. 7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability [O] . Francesco Paduano, Emma Colao, Sara Loddo, 2020

机译：7Q35微缺失和15Q13.3和XP22.33微量件在患者中严重的肌阵挛性癫痫，微头畸形，虚张声势，严重的精神接受延迟和智力残疾

A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach

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