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 Delezioni Rare Presso Il Locus Neurexin 3 Nel Disturbo Dello Spettro Autistico American Journal of Human Genetics. Jan, 2012 | Pubmed ID: 22209245 Risultati Inaspettati in Geni Di Predisposizione Del Cancro Rilevati Dall'ibridazione Genomic Comparativa Matrice: Quali Sono I Problemi? Journal of Medical Genetics. Aug, 2011 | Pubmed ID: 21429933 MLPA Per Conferma Dei Risultati CGH Array E Determinazione Dell'ereditarietà Molecular Cytogenetics. 2010 | Pubmed ID: 20942916 Validazione E Implementazione Di Ibridazione Genomic Comparativa Di Matrice Come Prima Linea Di Test Al Posto Del Cariotipo Postnatale Per Lo Squilibrio Del Genoma Molecular Cytogenetics. 2010 | Pubmed ID: 20398301 Una Romanzo Cancellazione in 22q Prossimale Associato Con Difetti Del Setto Cardiaci E Microcefalia: Un Rapporto Di Caso Molecular Cytogenetics. 2009 | Pubmed ID: 19239688 Squilibrio Cromosomiche Submicroscopiche in Pazienti Con Ritardo Di Sviluppo E/o Dismorfismi Indicato Specificamente Per L'analisi Di Test E Cariotipo X Fragile Molecular Cytogenetics. 2008 | Pubmed ID: 18471307 Rilevamento Di Squilibrio Subtelomeriche Mediante MLPA: Convalida, Lo Sviluppo Di Un Protocollo Di Analisi E L'applicazione in Un Centro Diagnostico BMC Medical Genetics. 2007 | Pubmed ID: 17338807 Gammaherpesvirus Lytic Gene Expression As Characterized by DNA Array Journal of Virology. Jun, 2002 | Pubmed ID: 12021358 Array Comparative Genomic Hybridization (CGH Array) per il rilevamento di Genomic Copy Number Varianti 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 Biology
Array Comparative Genomic Hybridization (CGH Array) per il rilevamento di Genomic Copy Number Varianti 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 Biology