A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non-coding element

Author:

Justice Cristina M.1ORCID,Kim Jinoh23,Kim Sun-Don2,Kim Kyunhgho2,Yagnik Garima2,Cuellar Araceli2,Carrington Blake4,Lu Chung-Ling23,Sood Raman4,Boyadjiev Simeon A.2,Wilson Alexander F.1

Affiliation:

1. Genometrics Section; Computational and Statistical Genomics Branch; National Human Genome Research Institute; National Institutes of Health; Baltimore Maryland

2. Division of Genomic Medicine; Department of Pediatrics; University of California Davis Medical Center; Sacramento California

3. Department of Biomedical Sciences; Iowa State University; Ames Iowa

4. Zebrafish Core; Translational and Functional Genomics Branch; National Human Genome Research Institute; National Institutes of Health; Bethesda Maryland

Funder

Children's Miracle Network Endowed Chair

National Institute of Dental and Craniofacial Research

National Human Genome Research Institute

National Institute of General Medical Sciences

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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