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Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2, BBS7, and EVC2 Mutations.
Kantaputra, Piranit; Dejkhamron, Prapai; Sittiwangkul, Rekwan; Katanyuwong, Kamornwan; Ngamphiw, Chumpol; Sonsuwan, Nuntigar; Intachai, Worrachet; Tongsima, Sissades; Beales, Philip L; Buranaphatthana, Worakanya.
Afiliación
  • Kantaputra P; Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Chiang Mai 50200, Thailand.
  • Dejkhamron P; Dentaland Clinic, Chiang Mai 50200, Thailand.
  • Sittiwangkul R; Center of Excellence in Medical Genetics Research, Faculty of Dentistry, Chiang Mai University, Chiang Mai 50200, Thailand.
  • Katanyuwong K; Division of Pediatric Endocrinology, Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
  • Ngamphiw C; Division of Pediatric Cardiology, Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
  • Sonsuwan N; Division of Pediatric Neurology, Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
  • Intachai W; National Biobank of Thailand, National Science and Technology Development Agency, Pathum Thani 12120, Thailand.
  • Tongsima S; Department of Otolaryngology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
  • Beales PL; Center of Excellence in Medical Genetics Research, Faculty of Dentistry, Chiang Mai University, Chiang Mai 50200, Thailand.
  • Buranaphatthana W; National Biobank of Thailand, National Science and Technology Development Agency, Pathum Thani 12120, Thailand.
Genes (Basel) ; 14(1)2022 12 27.
Article en En | MEDLINE | ID: mdl-36672825
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Dentarias / Síndrome de Ellis-Van Creveld / Síndrome de Bardet-Biedl Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Tailandia
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Dentarias / Síndrome de Ellis-Van Creveld / Síndrome de Bardet-Biedl Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Tailandia