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Paper Details

Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.
Am J Med Genet A
2
2022
A/M, Anophthalmia, Birth Defects, DNA samples, PAX6, anophthalmia, birth defects, candidate genes, human, infants, microphthalmia, vision loss
Author NameAffiliation
Jingjing LiDepartment of Neurology School of Medicine, The Bakar Computational Health Sciences Institute, The Parker Institute for Cancer Immunotherapy, University of California San Francisco
Deborah A NickersonUniversity of Washington
Deborah A NickersonBrotman Baty Institute for Precision Medicine
Deborah A NickersonUniversity of Washington
Deborah A NickersonBrotman Baty Institute for Precision Medicine
Jessica X ChongUniversity of Washington
Jessica X ChongUniversity of Washington
Jessica X ChongBrotman Baty Institute for Precision Medicine
Jessica X ChongBrotman Baty Institute for Precision Medicine
James C MullikinNational Human Genome Research Institute, National Institutes of Health
James C MullikinNational Human Genome Research Institute, National Institutes of Health
Wendy N NembhardFay W. Boozman College of Public Health, University of Arkansas for Medical Sciences
Andrew F OlshanUniversity of North Carolina at Chapel Hill
Richard H FinnellCenter for Precision Environmental Health, Baylor College of Medicine
Richard H FinnellCenter for Precision Environmental Health, Baylor College of Medicine
Richard H FinnellCenter for Precision Environmental Health, Baylor College of Medicine
Michael J BamshadUniversity of Washington
Michael J BamshadUniversity of Washington
Michael J BamshadBrotman Baty Institute for Precision Medicine
Michael J BamshadUniversity of Washington
Michael J BamshadBrotman Baty Institute for Precision Medicine
Michael J BamshadUniversity of Washington
Lawrence C BrodyNational Human Genome Research Institute, National Institutes of Health
Lawrence C BrodyNational Human Genome Research Institute, National Institutes of Health
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