Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, USA
Seattle Children’s Hospital, Seattle, USA
Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, USA;
Sonora Quest Laboratories, Tempe, USA
Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, USA
Victorian Cancer Cytogenetics Service, St. Vincent’s Hospital Melbourne, Fitzroy, Australia
Genetics Associates, Inc., Nashville, USA
Johns Hopkins University School of Medicine, Baltimore, USA
Pathology Associates Medical Laboratories (PAML), Spokane, USA
Fred Hutchinson Cancer Research Center, Seattle, USA
Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, USA
Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, USA
Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, USA
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, USA
Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, USA
Paw Print Genetics, Genetic Veterinary Sciences, Inc., Spokane, USA
Magee-Womens Hospital, University of Pittsburgh Medical Center, Pittsburgh, USA
Empire Genomics, Buffalo, USA
Paw Print Genetics, Genetic Veterinary Sciences, Inc., Spokane, USA
Paw Print Genetics, Genetic Veterinary Sciences, Inc., Spokane, USA
Copyright © 2013 Roger A. Schultz, Karen Tsuchiya, Aubry Furrow, Marilyn L. Slovak, Lisa D. McDaniel, Meaghan Wall, Eric Crawford, Yi Ning, Reza Saleki, Min Fang, Victoria Cawich, Caitlin E. Johnson, Sara L. Minier, Nicholas J. Neill, S. Annie Morton, Steve Byerly, Urvashi Surti, Theresa C. Brown, Blake C. Ballif, Lisa G. Shaffer et al. This is
an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any
medium, provided the original work is properly cited.
How to Cite this Article
Schultz, R. , Tsuchiya, K. , Furrow, A. , Slovak, M. , McDaniel, L. , Wall, M. , Crawford, E. , Ning, Y. , Saleki, R. , Fang, M. , Cawich, V. , Johnson, C. , Minier, S. , Neill, N. , Morton, S. , Byerly, S. , Surti, U. , Brown, T. , Ballif, B. and Shaffer, L. (2013) CGH-based microarray detection of cryptic and novel copy number alterations and balanced translocations in cytogenetically abnormal cases of b-cell all.
Health,
5, 23-40. doi:
10.4236/health.2013.55A004.