Consensus-based detection of aetiologic copy number variants for syndromic orofacial clefts utilising whole exome sequencing of case parent trios
2026BMC Genomic DataJournalOpen access
10.1186/s12863-026-01466-yFull text0 citations
2026BMC Genomic DataJournalOpen access
10.1186/s12863-026-01466-yFull text0 citations
10 authors across 3 institutions in 2 countries.
Assignment is probabilistic — a work belongs to several fields in proportions.
Several sources describing one work is the point — it means the record rests on more than one authority.
2026 · BMC Genomic Data · 0 citations
https://openalex.org/W7167678947