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BMC Pediatrics|June 12, 2012
Relational development in children with cleft lip and palate: influence of the waiting period prior to the first surgical intervention and parental psychological perceptions of the abnormalityBruno Grollemund, Antoine Guedeney, Marie-Paule Vazquez, et al.Human Pathology|January 16, 2013
PTCH1 mutation and local aggressiveness of odontogenic keratocystic tumors in children: is there a relationship?Natacha Kadlub, Amélie Coudert, Marie-Eve Gatibelza, et al.Sleep & Breathing = Schlaf & Atmung|June 6, 2024
Management of sleep-disordered breathing in patients with syndromic hemifacial macrosomiaBarbara Madini, Sonia Khirani, Meryl Vedrenne-Cloquet, et al.American Journal of Medical Genetics. Part A|January 30, 2023
An automatic facial landmarking for children with rare diseasesQuentin Hennocq, Thomas Bongibault, Matthieu Bizière, et al.Orphanet Journal of Rare Diseases|April 19, 2023
Craniofacial growth and function in achondroplasia: a multimodal 3D study on 15 patientsAnne Morice, Maxime Taverne, Sophie Eché, et al.Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|June 1, 2013
Specificity of paediatric jawbone lesions: tumours and pseudotumoursNatacha Kadlub, Tamara Kreindel, Valère Belle Mbou, et al.Journal of Medical Genetics|September 4, 2023
Biallelic truncating variants in <i>VGLL2</i> cause syngnathia in humansValeria Agostini, Aude Tessier, Nabila Djaziri, et al.Journal of Medical Genetics|July 1, 2016
Mutations in <i>MYT1</i>, encoding the myelin transcription factor 1, are a rare cause of OAVSEstelle Lopez, Marie Berenguer, Angèle Tingaud-Sequeira, et al.The Journal of Investigative Dermatology|October 17, 2013
NRAS mutation is the sole recurrent somatic mutation in large congenital melanocytic neviChristelle Charbel, Romain H Fontaine, Gabriel G Malouf, et al.Prenatal Diagnosis|April 18, 2024
Artificial intelligence-based diagnosis in fetal pathology using external ear shapesQuentin Hennocq, Nicolas Garcelon, Thomas Bongibault, et al.Pageof 11