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Paper Details

Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis.
Genes (Basel)
3
2022
20p12, 20q13, 20q13.2-q13, 3q29, 7p14, CS, Candidate Regions, Craniosynostosis, GWAS variant, Sagittal and Metopic Nonsyndromic Craniosynostosis, binding sites, birth defect, candidate genes, child, imputed variants, mNCS, metopic non-syndromic NCS, non-syndromic CS, rs1884302, rs1884302 C, rs6127972, rs6127972 T allele, sNCS
Author NameAffiliation
Justin PaschallNational Human Genome Research Institute, National Institute of Health (NIH)
Justin PaschallNational Human Genome Research Institute, National Institute of Health (NIH)
Andrew O M WilkieMRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital
Andrew O M WilkieOxford University Hospitals NHS Foundation Trust
Andrew O M WilkieOxford University Hospitals NHS Foundation Trust
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Release 1.2