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Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate

Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common congenital birth defects. NSCL/P is a complex multifactorial disease caused by interactions between multiple environmental and genetic factors. However, the causal single nucleotide polymorphism (SNP) signature pr...

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Bibliographische Detailangaben
Veröffentlicht in:Front Genet
Hauptverfasser: Mitra, Amit K., Stessman, Holly A. F., Schaefer, Robert J., Wang, Wen, Myers, Chad L., Van Ness, Brian G., Beiraghi, Soraya
Format: Artigo
Sprache:Inglês
Veröffentlicht: Frontiers Media S.A. 2016
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4876112/
https://ncbi.nlm.nih.gov/pubmed/27242896
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2016.00088
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