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 Matriz Hibridização Genômica Comparativa (Array CGH) para a detecção de Genomic copiar o número de variantes 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
Matriz Hibridização Genômica Comparativa (Array CGH) para a detecção de Genomic copiar o número de variantes 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