Single-Nucleotide Polymorphisms in
WNT
birth defect
cleft lip
cleft palate
genetic variation
orofacial cleft
polymorphism
Journal
Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402
Informations de publication
Date de publication:
17 Jul 2024
17 Jul 2024
Historique:
received:
28
05
2024
revised:
04
07
2024
accepted:
15
07
2024
medline:
27
7
2024
pubmed:
27
7
2024
entrez:
27
7
2024
Statut:
epublish
Résumé
Non-syndromic orofacial cleft (OFC) is the most common facial developmental defect in the global population. The etiology of these birth defects is complex and multifactorial, involving both genetic and environmental factors. This study aimed to determine if SNPs in the
Identifiants
pubmed: 39061674
pii: diagnostics14141537
doi: 10.3390/diagnostics14141537
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : National Science Center
ID : 2169/B/P01/2011/40