Cephalometric assessment of craniofacial dysmorphologies in relation with Msx2 mutations in mouse

Author:

Simon Y.123,Marchadier A.2,Riviere M. K.4,Vandamme K.5,Koenig F.2,Lezot F.16,Trouve A.7,Benhamou C. L.2,Saffar J. L.3,Berdal A.189,Nefussi J. R.189

Affiliation:

1. Team 5; UMRS 872 INSERM; Paris France

2. INSERM; U 658-IPROS CHR Orléans BP 2439; Orléans Cedex 1 France

3. Dental School; University Paris 5 Descartes; Paris France

4. INSERM; U872; Centre de recherche des Cordeliers; Université Paris 5; Université Paris 6; Paris France

5. CNRS; UMR 7052 B2OA; University Paris Diderot; Paris France

6. INSERM UMR957; Faculty of Medicine; Nantes University; Nantes France

7. CMLA; ENS de Cachan; Cachan Cedex France

8. Dental School; University Paris 7 Diderot; Paris France

9. Service d'Odontologie; AP-HP Hopital Rotchschild; Paris France

Publisher

Wiley

Subject

Otorhinolaryngology,Oral Surgery,Surgery,Orthodontics

Reference25 articles.

1. Craniofacial Development The Tissue and Molecular Interactions That Control Development of the Head

2. Msx homeobox gene family and craniofacial development;Alappat;Cell Res,2003

3. Expression patterns of the homeobox gene, Hox-8, in the mouse embryo suggest a role in specifying tooth initiation and shape;MacKenzie;Development,1992

4. Differential impact of MSX1 and MSX2 homeogenes on mouse maxillofacial skeleton;Berdal;Cells Tissues Organs,2009

5. Msx1 is a regulator of bone formation during development and postnatal growth: in vivo investigations in a transgenic mouse model;Orestes-Cardoso;Connect Tissue Res,2002

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