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
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

Auteurs

Alicja Zawiślak (A)

Department of Interdisciplinary Dentistry, Pomeranian Medical University, 70-111 Szczecin, Poland.
Department of Maxillofacial Orthopaedics and Orthodontics, Institute of Mother and Child, 01-211 Warsaw, Poland.

Krzysztof Woźniak (K)

Department of Orthodontics, Pomeranian Medical University, 70-111 Szczecin, Poland.

Gianluca Tartaglia (G)

Department of Biomedical, Surgical and Dental Sciences, University of Milan, 20122 Milan, Italy.

Xabier Agirre (X)

Centro de Investigación Médica Aplicada, IDISNA, Universidad de Navarra, Avenida Pío XII-55, 31008 Pamplona, Spain.

Satish Gupta (S)

Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland.

Beata Kawala (B)

Department of Dentofacial Orthopaedics and Orthodontics, Wrocław Medical University, 50-425 Wrocław, Poland.

Anna Znamirowska-Bajowska (A)

Department of Dentofacial Orthopaedics and Orthodontics, Wrocław Medical University, 50-425 Wrocław, Poland.

Katarzyna Grocholewicz (K)

Department of Interdisciplinary Dentistry, Pomeranian Medical University, 70-111 Szczecin, Poland.

Felipe Prosper (F)

Centro de Investigación Médica Aplicada, IDISNA, Universidad de Navarra, Avenida Pío XII-55, 31008 Pamplona, Spain.

Jan Lubiński (J)

Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland.

Anna Jakubowska (A)

Laboratory of Molecular Biology and Genetic Diagnostics, Pomeranian Medical University, 70-111 Szczecin, Poland.

Classifications MeSH