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An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

机译：启发式过滤工具，用于识别与表型相关的遗传变异，将其应用于人类智力障碍和犬毛颜色

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Bart J. G. Broeckx; Frank Coopman; Geert Verhoeven; Tim Bosmans; Ingrid Gielen; Walter Dingemanse; Jimmy H. Saunders; Dieter Deforce; Filip Van Nieuwerburgh;
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1. An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors [J] . Bart J. G. Broeckx, Frank Coopman, Geert Verhoeven, BMC Bioinformatics . 2015,第1期

机译：一种启发式过滤工具，用于识别应用于人类智力残疾和犬毛颜色的与表型相关的遗传变异
2. Recurrent benign copy number variants & issues in interpretation of variants of unknown significance identified by cytogenetic microarray in Indian patients with intellectual disability [J] . Boggula Vijay Raju, Agarwal Meenal, Kumar Rashmi, The Indian journal of medical research. . 2015,第1期

机译：复发性良性拷贝数变异和印度遗传性智力障碍患者通过细胞遗传芯片鉴定未知意义变异的解释中的问题
3. Recurrent benign copy number variants & issues in interpretation of variants of unknown significance identified by cytogenetic microarray in Indian patients with intellectual disability [J] . Vijay Raju Boggula, Meenal Agarwal, Rashmi Kumar, The Indian journal of medical research . 2015,第6期

机译：印度智力障碍患者的复发性良性拷贝数变异和通过细胞遗传芯片鉴定的意义不明变异的解释中的问题
4. Variant-DB: A Tool for Efficiently Exploring Millions of Human Genetic Variants and Their Annotations [C] . Joachim Kutzera, Patrick May International conference on data integration in the life sciences . 2017

机译：Variant-DB：一种有效探索数百万人类遗传变异及其注释的工具
5. Use of Q-Methodology to Identify Clinical Psychologists' Attitudes Towards Genetic Research Affecting People With Intellectual and Developmental Disabilities [D] . Vahey, Catherine. 2013

机译：使用Q方法论来确定临床心理学家对影响智力和发育障碍者的基因研究的态度
6. An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors [O] . Bart J. G. Broeckx, Frank Coopman, Geert Verhoeven, 2015

机译：启发式过滤工具用于识别与表型相关的遗传变异将其应用于人类智力障碍和犬毛颜色
7. Recurrent benign copy number variants & issues in interpretation of variants of unknown significance identified by cytogenetic microarray in Indian patients with intellectual disability [O] . Vijay Raju Boggula, Meenal Agarwal, Rashmi Kumar, 2015

机译：复发性良性拷贝数变异及解释印度智力障碍患者细胞遗传学微阵列鉴定的未知重要变异的问题
8. Human Cholinesterase Gene Expression in Mammalian Cells: Proposed Nomenclaturefor Human Butyrylcholinesterase Genetic Variants Identified by DNA Sequencing [R] . Lockridge, O., La Du, B. N., Bartels, C. F., 1991

机译：人类胆碱酯酶基因在哺乳动物细胞中的表达：通过DNa测序鉴定的人丁酰胆碱酯酶遗传变异的拟议命名法

An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

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