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G Baujat

Showing results (11-20 of 35) with videos related to

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Annals of the Rheumatic Diseases|October 1, 2015
Mutation in MMP2 gene may result in scleroderma-like skin thickeningB Bader-Meunier, L Bonafé, S Fraitag, et al.
Hormone Research|April 26, 2003
Adrenal insufficiency and abnormal genitalia in a 46XX female with Smith-Lemli-Opitz syndromeW Chemaitilly, A Goldenberg, G Baujat, et al.
The British Journal of Oral & Maxillofacial Surgery|May 2, 2016
Re: Agarwal et al Stylomandibular fusion that complicates recurrent bilateral ankylosis of the temporomandibular jointP Nicol, B Ruhin, S Sourice, et al.
American Journal of Medical Genetics. Part A|May 19, 2009
Congenital skin pedicles with or without amniotic band sequence: Extending the human phenotype resembling mouse disorganizationB Isidor, G Baujat, C Le Caignec, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial|February 7, 2004
[Epidemiology and prognosis of childhood cancers in Dakar, Senegal]A S Ka, P Imbert, C Moreira, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 26, 2018
Enzyme-replacement therapy in perinatal hypophosphatasia: Case report and review of the literatureH Rougier, A Desrumaux, N Bouchon, et al.
Neuro-Chirurgie|September 29, 2019
Craniosynostosis and metabolic bone disorder. A reviewF Di Rocco, A Rothenbuhler, V Cormier Daire, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 19, 2017
[Transverse reductional anomaly and atypical fibrodysplasia ossificans progressiva: A case diagnosed late]J Paysal, C Sarret, E Merlin, et al.
American Journal of Medical Genetics. Part A|August 2, 2008
Molecular study of 33 families with Fraser syndrome new data and mutation reviewM M van Haelst, M Maiburg, G Baujat, et al.
Journal of Stomatology, Oral and Maxillofacial Surgery|January 15, 2019
Gnathodiaphyseal dysplasia with a novel R597I mutation of ANO5: Mandibular reconstruction strategiesG Marechal, T Schouman, C Mauprivez, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Annals of the Rheumatic Diseases|October 1, 2015
Mutation in MMP2 gene may result in scleroderma-like skin thickeningB Bader-Meunier, L Bonafé, S Fraitag, et al.
Hormone Research|April 26, 2003
Adrenal insufficiency and abnormal genitalia in a 46XX female with Smith-Lemli-Opitz syndromeW Chemaitilly, A Goldenberg, G Baujat, et al.
The British Journal of Oral & Maxillofacial Surgery|May 2, 2016
Re: Agarwal et al Stylomandibular fusion that complicates recurrent bilateral ankylosis of the temporomandibular jointP Nicol, B Ruhin, S Sourice, et al.
American Journal of Medical Genetics. Part A|May 19, 2009
Congenital skin pedicles with or without amniotic band sequence: Extending the human phenotype resembling mouse disorganizationB Isidor, G Baujat, C Le Caignec, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial|February 7, 2004
[Epidemiology and prognosis of childhood cancers in Dakar, Senegal]A S Ka, P Imbert, C Moreira, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 26, 2018
Enzyme-replacement therapy in perinatal hypophosphatasia: Case report and review of the literatureH Rougier, A Desrumaux, N Bouchon, et al.
Neuro-Chirurgie|September 29, 2019
Craniosynostosis and metabolic bone disorder. A reviewF Di Rocco, A Rothenbuhler, V Cormier Daire, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 19, 2017
[Transverse reductional anomaly and atypical fibrodysplasia ossificans progressiva: A case diagnosed late]J Paysal, C Sarret, E Merlin, et al.
American Journal of Medical Genetics. Part A|August 2, 2008
Molecular study of 33 families with Fraser syndrome new data and mutation reviewM M van Haelst, M Maiburg, G Baujat, et al.
Journal of Stomatology, Oral and Maxillofacial Surgery|January 15, 2019
Gnathodiaphyseal dysplasia with a novel R597I mutation of ANO5: Mandibular reconstruction strategiesG Marechal, T Schouman, C Mauprivez, et al.
Pageof 4