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Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|December 25, 2017
Orbital volume and shape in Treacher Collins syndromeJulie Levasseur, Johan Nysjö, Ronak Sandy, et al.
Frontiers in Pediatrics|December 8, 2018
Severity of Retrognathia and Glossoptosis Does Not Predict Respiratory and Feeding Disorders in Pierre Robin SequenceAnne Morice, Véronique Soupre, Delphine Mitanchez, et al.
Experimental Dermatology|May 20, 2016
Varying proliferative and clonogenic potential in NRAS-mutated congenital melanocytic nevi according to sizeSarah Guégan, Natacha Kadlub, Arnaud Picard, et al.
Orphanet Journal of Rare Diseases|June 12, 2026
Exploring a cherubism bone phenotype outside the craniofacial regionAnne Morice, Philippe Drabent, Sylvie Thomasseau, et al.
Journal of the American Academy of Dermatology|October 22, 2011
Connective tissue nevi: an entity revisitedAnne Saussine, Karine Marrou, Phillippe Delanoé, et al.
The Journal of Investigative Dermatology|May 7, 2019
Local Inhibition of MEK/Akt Prevents Cellular Growth in Human Congenital Melanocytic NeviThomas Rouillé, Selim Aractingi, Natacha Kadlub, et al.
Fetal Diagnosis and Therapy|February 28, 2023
Imaging Factors Affecting Prenatal Counseling in Orofacial CleftsAnne-Laure Hermann, Veronique Soupre, Saskia Vande Perre, et al.
The Journal of Investigative Dermatology|October 14, 2014
Clonogenic cell subpopulations maintain congenital melanocytic neviChristelle Charbel, Romain H Fontaine, Natacha Kadlub, et al.
Orphanet Journal of Rare Diseases|June 6, 2019
Oral health related quality of life of children and adolescents affected by rare orofacial diseases: a questionnaire-based cohort studyLisa Friedlander, Ariane Berdal, Priscilla Boizeau, et al.
European Journal of Medical Genetics|January 4, 2011
A new 17p13.3 microduplication including the PAFAH1B1 and YWHAE genes resulting from an unbalanced X;17 translocationCapucine Hyon, Sandrine Marlin, Sandra Chantot-Bastaraud, et al.
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