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Rare variants in embryonic development and cell signalling genes in syndromic and non-syndromic orofacial clefts: evidence from a Colombian Caribbean cohort.

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Bibliographic Details
Title: Rare variants in embryonic development and cell signalling genes in syndromic and non-syndromic orofacial clefts: evidence from a Colombian Caribbean cohort.
Authors: Silva A; Human Genetics and Genomic Medicine, University of Southampton, Southampton, UK. Alejandro.Silva-Espinosa@soton.ac.uk.; Grupo de Genética Humana, Facultad de Medicina-Universidad de La Sabana, Chía, Colombia. Alejandro.Silva-Espinosa@soton.ac.uk., Jaramillo Oquendo C; Human Genetics and Genomic Medicine, University of Southampton, Southampton, UK., Bernal JE; Grupo Genoma-Facultad de Medicina, Universidad del Sinú, Cartagena, Colombia., Martinez JC; Grupo de Genética Humana, Facultad de Medicina-Universidad de La Sabana, Chía, Colombia., Collins A; Human Genetics and Genomic Medicine, University of Southampton, Southampton, UK., Briceño I; Grupo de Genética Humana, Facultad de Medicina-Universidad de La Sabana, Chía, Colombia., Benavides E; Grupo Genoma-Facultad de Medicina, Universidad del Sinú, Cartagena, Colombia., López Arrieta Z; Grupo Genoma-Facultad de Medicina, Universidad del Sinú, Cartagena, Colombia., Ennis S; Grupo de Genética Humana, Facultad de Medicina-Universidad de La Sabana, Chía, Colombia. s.ennis@soton.ac.uk.
Source: Journal of human genetics [J Hum Genet] 2026 Jul; Vol. 71 (7), pp. 443-451. Date of Electronic Publication: 2026 Mar 30.
Publication Type: Journal Article
Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-232X (Electronic) Linking ISSN: 14345161 NLM ISO Abbreviation: J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1435-232X
DOI:10.1038/s10038-026-01466-x