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Re-focusing on Agnathia-Otocephaly complex.
Dubucs, C; Chassaing, N; Sergi, C; Aubert-Mucca, M; Attié-Bitach, T; Lacombe, D; Thauvin-Robinet, C; Arpin, S; Perez, M J; Cabrol, C; Chen, C P; Aziza, J; Colin, E; Martinovic, J; Calvas, P; Plaisancié, Julie.
Affiliation
  • Dubucs C; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.
  • Chassaing N; Département d'Anatomie et de Cytologie Pathologiques, Institut Universitaire du cancer de Toulouse, Toulouse, France.
  • Sergi C; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.
  • Aubert-Mucca M; INSERM U1056, Université Toulouse III, Toulouse, France.
  • Attié-Bitach T; Department of Lab. Med. & Pathology (5B4.09), University of Alberta, Edmonton, AB, Canada.
  • Lacombe D; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.
  • Thauvin-Robinet C; Unité d'Embryofœtopathologie, Service d'Histologie Embryologie Cytogénétique, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.
  • Arpin S; Institut Imagine, INSERM U1163, Université Paris Descartes, Sorbonne Paris Cite, Paris, France.
  • Perez MJ; Service de Génétique Médicale, CRMR, CHU de Bordeaux, Bordeaux, France.
  • Cabrol C; INSERM U1211, Université de Bordeaux, 33076, Bordeaux, France.
  • Chen CP; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
  • Aziza J; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon, Dijon, Bourgogne, France.
  • Colin E; Centre de Référence maladies rares "Anomalies du Développement et syndromes malformatifs," Centre de Génétique, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
  • Martinovic J; Service de Génétique Clinique, Centre Hospitalier Régional Universitaire de Tours, Tours, France.
  • Calvas P; Department of Medical Genetics, Reference Center for Developmental Abnormalities and Constitutional Bone Diseases, CHRU, Montpellier, France.
  • Plaisancié J; Centre de Génétique Humaine, Centre Hospitalier Universitaire, Université de Franche-Comté, Besançon, France.
Clin Oral Investig ; 25(3): 1353-1362, 2021 Mar.
Article in En | MEDLINE | ID: mdl-32643087
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Craniofacial Abnormalities / Jaw Abnormalities Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Clin Oral Investig Journal subject: ODONTOLOGIA Year: 2021 Document type: Article Affiliation country: France Country of publication: Germany
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Craniofacial Abnormalities / Jaw Abnormalities Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Clin Oral Investig Journal subject: ODONTOLOGIA Year: 2021 Document type: Article Affiliation country: France Country of publication: Germany