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Paper Details

Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes.
Am J Hum Genet
3
2023
ARHGEF38, CL/P, CNV, CNVs, COBLL1, CRISPR, Cas9, Cleft lip, Danio rerio, Mendelian clefting loci, RIC1, Xenopus laevis, birth defect, cleft lip and, cleft palate, clefting disorders, clefting genes, clefting loci, clefts, copy, copy-number variants, craniofacial dysmorphologies, genome-wide CNV, human, humans, non-syndromic, non-syndromic clefting, rare sequence variants, syndromic and non-syndromic Mendelian clefting, syndromic and non-syndromic Mendelian clefting loci, syndromic clefts
Author NameAffiliation
Nanette R LeeOffice of Population Studies Foundation, Inc., University of San Carlos
Karen L MohlkeUniversity of North Carolina
Santhosh GirirajanPennsylvania State University, University Park
Robert A CornellUniversity of Iowa
Robert A CornellUniversity of Iowa
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