P593: Detection of single-gene copy-number variations through high-resolution exon-targeted chromosomal microarray analysis
Matthew Hoi Kin Chau(Chinese University of Hong Kong), Weimin Bi(Zhejiang A & F University), Nichole Owen(Baylor College of Medicine), Liesbeth Vossaert(Baylor College of Medicine), Stephanie A. Anderson(Baylor Genetics), Sau Wai Cheung(Chinese University of Hong Kong), Katharina Schulze(Baylor College of Medicine), Paweł Stankiewicz(Baylor College of Medicine), Rodger Song(Baylor Genetics), Bo Yuan(Second Military Medical University), Janice Smith(Baylor Genetics), Yue Wang(Virginia Tech), Lance Cooper(Baylor Genetics), Patricia A. Ward(Baylor College of Medicine), Carlos A. Bacino(Baylor College of Medicine)
Cited by 1
Related Papers
Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
|New England Journal of Medicine|2013|2k
Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation
|New England Journal of Medicine|2016|774
Copy number analysis indicates monoclonal origin of lethal metastatic prostate cancer
|Nature Medicine|2009|666