Search Thermo Fisher Scientific
- Order Status
- Quick Order
-
Don't have an account ? Create Account
Search Thermo Fisher Scientific
Please refer to below resources to make the most out of your prenatal research applications. Hear from current customers, watch webinars, blog posts and much more.
Challenging microarray cases and the approaches for analysis of unusual findings
By Dr. Stuart Schwartz, Labcorp
Determining the genetic cause of disease by application of exon-level array as a complement to exome sequencing
By Dr. Benjamin Hilton, Greenwood Genetics Center
Case #1 Hybrid SNP array analysis in action: a practical approach to complex problems in the era of NGS
By Dr. Catherine Rehder, Duke University
SNP Chromosomal Microarray, the allelic difference
By Dr. Elizabeth McCready, McMaster University
Case #2 Hybrid SNP array analysis in action: a practical approach to complex problems in the era of NGS
By Dr. Kristen Deak, Duke University
Case #3 Hybrid SNP array analysis in action: a practical approach to complex problems in the era of NGS
By Dr. Kristen Deak, Duke University
Using hybrid-SNP microarrays to delineate UPD in cytogenetic samples
Dr. Stuart Schwartz, Labcorp
Clinical diagnosis of developmental disorders with chromosomal microarrays
Dr. Barbara DuPont, Senior Director, Cytogenetics Laboratory, Greenwood Genetic Center
CMA compares with conventional karyotyping in prenatal screening
Dr. Panyu Panburana, Dr. Takol Chareon-sirisuthigul and Dr. Thipwimol Tim-Aroon,Ramathibodi Hospital, Mahidol University
For Research Use Only. Not for use in diagnostic procedures.