DICER1 deletion and 14q32 microdeletion syndrome: an additional case and a review of the literature

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DICER1 deletion and 14q32 microdeletion syndrome: an additional case and a review of the literature

机译：DICER1缺失和14q32微缺失综合征：另一例并文献复习

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《Clinical dysmorphology 》 |2016年第1期| 共4页
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中图分类妇产科学 ;
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1. DICER1 deletion and 14q32 microdeletion syndrome: an additional case and a review of the literature [J] . Clinical dysmorphology . 2016 ,第1期

机译：DICER1缺失和14q32微缺失综合征：另一例并文献复习
2. An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literature. [J] . L Ng IS, Chin WH, P Lim EC, Twin research and human genetics : . 2011 ,第4期

机译：另一例复发的15q24.1微缺失综合征病例和文献复习。
3. Siblings with phenotypic overlap with Toriello-Carey syndrome and complex cytogenetic imbalances including 3q29 microduplication and 6p25 microdeletion: Review of the literature and additional evidence for genetic heterogeneity. [J] . McGoey R, Varma A, Lacassie Y American journal of medical genetics, Part A . 2010 ,第12期

机译：具有Toriello-Carey综合征的表型重叠的兄弟姐妹和复杂的细胞遗传失衡，包括3q29微重复和6p25微缺失：文献综述和遗传异质性的其他证据。
4. An intelligent web-based system for the detection and visualization of biomarkers in Microdeletion and Microduplication Syndromes [C] . Konstantinos Stefanou, Christos Bellos, Georgios Stergios, IEEE International Conference on Bioinformatics and Bioengineering . 2020

机译：基于智能网络的系统，用于检测和可视化微缺失和微杂皮综合征中的生物标志物
5. Social Cognition as a Predictor of Psychotic Symptoms in 22q11.2 Microdeletion Syndrome. [D] . Jalbrzikowski, Maria Elizabeth. 2013

机译：社会认知作为22q11.2微缺失综合征精神病症状的预测因子。
6. Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis [O] . M. Fernanda Rozas, Felipe Benavides, Luis León, 2019

机译：22q11.2微缺失综合征的表型与缺失大小之间的关联：系统评价和荟萃分析
7. Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis [O] . M. Fernanda Rozas, Felipe Benavides, Luis León, 2019

机译：22Q11.2微外翻综合征中表型和缺失大小之间的关联：系统评价和荟萃分析

DICER1 deletion and 14q32 microdeletion syndrome: an additional case and a review of the literature

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