Joo Wook Ahn Cytogenetics Department Guy's & St Thomas' NHS Foundation Trust Biography Publications Institution JoVE Articles Joo Wook Ahn has not added a biography. If you are Joo Wook Ahn and would like to personalize this page please email our Author Liaison for assistance. Publications CHD2 Haploinsufficiency is Associated with Developmental Delay, Intellectual Disability, Epilepsy and Neurobehavioural Problems Journal of Neurodevelopmental Disorders. 2014 | Pubmed ID: 24834135 A New Direction for Prenatal Chromosome Microarray Testing: Software-targeting for Detection of Clinically Significant Chromosome Imbalance Without Equivocal Findings PeerJ. 2014 | Pubmed ID: 24795849 Phenotypic Features in Patients with 15q11.2(BP1-BP2) Deletion: Further Delineation of an Emerging Syndrome American Journal of Medical Genetics. Part A. Aug, 2014 | Pubmed ID: 24715682 Disruption of the ASTN2/TRIM32 Locus at 9q33.1 is a Risk Factor in Males for Autism Spectrum Disorders, ADHD and Other Neurodevelopmental Phenotypes Human Molecular Genetics. May, 2014 | Pubmed ID: 24381304 NRXN1 Deletions Identified by Array Comparative Genome Hybridisation in a Clinical Case Series - Further Understanding of the Relevance of NRXN1 to Neurodevelopmental Disorders Journal of Molecular Psychiatry. 2013 | Pubmed ID: 25408897 BBGRE: Brain and Body Genetic Resource Exchange Database : the Journal of Biological Databases and Curation. 2013 | Pubmed ID: 24077841 Male-biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders PloS One. 2013 | Pubmed ID: 23637818 Array CGH As a First Line Diagnostic Test in Place of Karyotyping for Postnatal Referrals - Results from Four Years' Clinical Application for over 8,700 Patients Molecular Cytogenetics. 2013 | Pubmed ID: 23560982 在自闭症谱系障碍 Neurexin 3 案发现场的罕见删除。 American Journal of Human Genetics. Jan, 2012 | Pubmed ID: 22209245 癌症易感性基因检测阵列比较基因组杂交中的意外的结果: 的问题是什么? Journal of Medical Genetics. Aug, 2011 | Pubmed ID: 21429933 洗钱法测定继承和数组计算全息图结果确认。 Molecular Cytogenetics. 2010 | Pubmed ID: 20942916 验证和执行的第一行作为阵列比较基因组杂交试验代替产后核型分析技术对基因组的不平衡。 Molecular Cytogenetics. 2010 | Pubmed ID: 20398301 新型缺失的关联与心脏间隔缺损和小头畸形的近端 22q: 病例的报告。 Molecular Cytogenetics. 2009 | Pubmed ID: 19239688 亚显微染色体不平衡患者发育迟缓和/或异形提到专门为脆性 X 测试和染色体核型分析。 Molecular Cytogenetics. 2008 | Pubmed ID: 18471307 使用洗钱法亚端粒不平衡检测: 验证、 分析议定书 》,并在诊断中心中的应用的发展。 BMC Medical Genetics. 2007 | Pubmed ID: 17338807 Gammaherpesvirus Lytic Gene Expression As Characterized by DNA Array Journal of Virology. Jun, 2002 | Pubmed ID: 12021358 阵列比较基因组杂交(CGH阵列),用于检测基因拷贝数变异的 Joo Wook Ahn1, Michael Coldwell2, Susan Bint2, Caroline Mackie Ogilvie1 1Cytogenetics Department, Guy's & St Thomas' NHS Foundation Trust, 2Cytogenetics Department, Viapath Analytics JoVE 51718 生物学
阵列比较基因组杂交(CGH阵列),用于检测基因拷贝数变异的 Joo Wook Ahn1, Michael Coldwell2, Susan Bint2, Caroline Mackie Ogilvie1 1Cytogenetics Department, Guy's & St Thomas' NHS Foundation Trust, 2Cytogenetics Department, Viapath Analytics JoVE 51718 生物学