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Paper Details

Recurrent Rare Copy Number Variants Increase Risk for Esotropia.
Invest Ophthalmol Vis Sci
6
2020
10:47049547-47703870, B allele, CNVs, Copy Number Variants, Esotropia, OR 11, chromosome 10q11, chromosome 2p11, chromosome 4p15, esotropia, hg19, hg19, 2:87428677, lncRNA, long, long noncoding RNA, microRNAs, patients, protein-coding genes, pseudogenes
Author NameAffiliation
James A KnowlesSUNY Downstate Health Sciences University
Chris ArmoskusSUNY Downstate Health Sciences University
Michele T PatoInstitute for Genomic Health, SUNY Downstate Medical Center
Carlos N PatoInstitute for Genomic Health, SUNY Downstate Medical Center
David A MackeyLions Eye Institute, University of Western Australia
David A MackeyMenzies Institute for Medical Research, University of Tasmania
David A MackeyUniversity of Melbourne
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