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European Journal of Medical Genetics|July 5, 2008
The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvementIsabelle Bailleul-Forestier, Ariane Berdal, Frans Vinckier, et al.
Case Reports in Dentistry|October 2, 2020
Gingival Biopsy to Detect Mosaicism in Overgrowth Syndromes: Report of Two Cases of Megalencephaly-Capillary Malformation Syndrome with Periodontal AnomaliesMathieu Marty, Carole Bonnaud, Natalie Jones, et al.
European Journal of Medical Genetics|April 24, 2012
Oral manifestations of patients with Kenny-Caffey SyndromeYoussra Moussaid, Didier Griffiths, Béatrice Richard, et al.
International Journal of Paediatric Dentistry|August 9, 2007
Caries experience in a severely obese adolescent populationIsabelle Bailleul-Forestier, Karine Lopes, Mourad Souames, et al.
Clinical Rheumatology|May 11, 2020
Orofacial manifestations of SAPHO syndrome: a systematic review of case reportsClémence Ferreira-Vilaca, Leonor Costa Mendes, Sophie-Caroline Campana, et al.
International Orthodontics|July 26, 2023
Association between malocclusions and amelogenesis imperfecta genotype and phenotype: A systematic reviewAlice Broutin, Angélique K Bidi-Lebihan, Thibault Canceill, et al.
American Journal of Medical Genetics. Part A|June 17, 2015
Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndromeSimon Poelmans, Tatsuro Kawamoto, Francesca Cristofoli, et al.
Clinical Genetics|February 6, 2020
LEF1 haploinsufficiency causes ectodermal dysplasiaJonathan Lévy, Yline Capri, Myriam Rachid, et al.
International Journal of Molecular Sciences|March 13, 2024
Structural Variant Disrupting the Expression of the Remote <i>FOXC1</i> Gene in a Patient with Syndromic Complex MicrophthalmiaJulie Plaisancié, Bertrand Chesneau, Lucas Fares-Taie, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndromeLaila Rifai, Marylin Port-Lis, Anne-Claude Tabet, et al.
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