Commentary on "Craniofacial Syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis".

Autor: Lecca M; Unit of Medical Genetics, Department of Molecular Medicine, University of Pavia, 27100, Pavia, Italy., Scribante A; Unit of Dental Hygiene, Section of Dentistry, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, 27100, Pavia, Italy.; Unit of Orthodontics and Pediatric Dentistry, Section of Dentistry, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, 27100, Pavia, Italy., Errichiello E; Unit of Medical Genetics, Department of Molecular Medicine, University of Pavia, 27100, Pavia, Italy. edoardo.errichiello@unipv.it.; Neurogenetics Research Center, IRCCS Mondino Foundation, 27100, Pavia, Italy. edoardo.errichiello@unipv.it.
Jazyk: angličtina
Zdroj: Pediatric research [Pediatr Res] 2024 May; Vol. 95 (6), pp. 1412-1414. Date of Electronic Publication: 2024 Jan 20.
DOI: 10.1038/s41390-024-03036-3
Databáze: MEDLINE
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