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Session 3 - Use of chromosome microarrays
4 June 2012, 1:15 pm - 3:15 pm
Americana Ballroom Salon 1

Featuring

Invited Presentations and Selected Abstracts (3-1 through 3-5)

 


Chair: Patricia Devers (United States) and Ronald Wapner (United States)
Array CGH in prenatal diagnosis: An overview
Ronald Wapner
Columbia University College of Physicians and Surgeons, USA
Array CGH in prenatal diagnosis: Genetic counseling issues
Patricia Devers
University of North Carolina, USA
3-1 The Use Of Chromosome Microarray Analysis As A First-Line Test In Low Risk Pregnancies
Francesco Fiorentino*1, Stefania Napoletano1, Fiorina Caiazzo1, Sara Bono1, Letizia Spizzichino1, Silvia Michiorri1, Anthony Gordon2, Andrea Nuccitelli1, Giuseppe Rizzo1, Mariateresa Sessa1, Marina Baldi1
1GENOMA”- Molecular Genetics Laboratory, Italy, 2Bluegnome Ltd, United Kingdom
3-2 Experience with Microarray Comparative Genomic Hybridization for Prenatal Diagnosis in Over 5,000 Pregnancies
Jill A Rosenfeld*1, Mindy P Dabell1, Allan J Fisher2, Justine Coppinger1, Anne Bandholz1, Jay W Ellison1, J Britt Ravnan1, Beth S Torchia1, Blake C Ballif1, Lisa G Shaffer1
1Signature Genomic Laboratories, PerkinElmer, Inc., United States, 2Commonwealth Perinatal Services, Henrico Doctors' Hospital, United States
3-3 Is Microarray Analysis Useful in Pregnancies with Abnormal Ultrasound Findings?
Lisa G Shaffer*1, Allan J Fisher2, Mindy P Dabell1, Justine Coppinger1, Anne Bandholz1, Jay W Ellison1, J Britt Ravnan1, Beth S Torchia1, Blake C Ballif1, Jill A Rosenfeld1
1Signature Genomic Laboratories, PerkinElmer, Inc., United States, 2Commonwealth Perinatal Services, Henrico Doctors' Hospital, United States
3-4 Prenatal Detection of Both Copy Number and Copy Neutral Changes by SNP Array Analysis.
Stuart Schwartz*1, Rachel Burnside1, Inder Gadi1, Elizabeth Keitges2, Romela Pasion1, Karen Phillips1, Venkatswara Potluri1, Hiba Risheg2, Brooke Rush1, Holly Taylor1, Jim Tepperberg1, Peter Papenhausen1
1Laboratory Corporation of America, Department of Cytogenetics, Center for Molecular Biology and Pathology,, United States, 2LabCorp/Dynacare, United States
3-5 Chromosome Microarray Analysis In Routine Prenatal Diagnosis Practice: A Prospective Study On 2800 Clinical Cases
Francesco Fiorentino*1, Fiorina Caiazzo1, Stefania Napoletano1, Letizia Spizzichino1, Sara Bono1, Silvia Michiorri1, Andrea Nuccitelli1, Anthony Gordon2, Giuseppe Rizzo1, Mariateresa Sessa1, Marina Baldi1
1GENOMA”- Molecular Genetics Laboratory, Italy, 2Bluegnome Ltd, United Kingdom