Susan Bint Cytogenetics Department Viapath Analytics Biography Publications Institution JoVE Articles Susan Bint has not added a biography. If you are Susan Bint and would like to personalize this page please email our Author Liaison for assistance. Publications 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 Meiotic Outcomes of Three-way Translocations Ascertained in Cleavage-stage Embryos: Refinement of Reproductive Risks and Implications for PGD European Journal of Human Genetics : EJHG. Jun, 2014 | Pubmed ID: 24129433 Multicolor Banding Remains an Important Adjunct to Array CGH and Conventional Karyotyping Molecular Cytogenetics. 2013 | Pubmed ID: 24314262 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 Successful PGD Cycles for Mosaic Robertsonian Translocation Carriers Provide Insights into the Mechanism of Formation of the Derivative Chromosomes American Journal of Medical Genetics. Part A. Mar, 2013 | Pubmed ID: 23401053 Tissue-specific Mosaicism for Tetrasomy 9p Uncovered by Array CGH American Journal of Medical Genetics. Part A. Oct, 2011 | Pubmed ID: 21998854 M-banding Characterization of a 16p11.2p13.1 Tandem Duplication in a Child with Autism, Neurodevelopmental Delay and Dysmorphism European Journal of Medical Genetics. Nov-Dec, 2008 | Pubmed ID: 18674645 Multicolor Banding Detects a Complex Three Chromosome, Seven Breakpoint Unbalanced Rearrangement in an ICSI-derived Fetus with Multiple Abnormalities American Journal of Medical Genetics. Part A. May, 2006 | Pubmed ID: 16596677 Class II Neocentromeres: a Putative Common Neocentromere Site in Band 4q21.2 European Journal of Human Genetics : EJHG. Oct, 2003 | Pubmed ID: 14512964 Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants 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 (Array CGH) for Detection of Genomic Copy Number Variants 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