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Annales De Chirurgie Plastique Et Esthetique
|
September 6, 2001
[Mandibular advancement: osteotomy or distraction osteogenesis? A case report]
P A Diner, C Tomat, V Soupre, et al.
Growth Regulation
|
December 1, 1991
Loss of heterozygosity in non-tumoral tissue in two children with Beckwith-Wiedemann syndrome
H Schneid, M P Vazquez, D Seurin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 26, 2011
[Congenital epulis: refrain from surgery. A case report of spontaneous regression]
N Kadlub, E Galliani, N Oker, et al.
Nucleic Acids Research
|
June 11, 1992
Nucleotide sequence of a cDNA encoding another Trypanosoma cruzi acidic ribosomal P2 type protein (TcP2b)
M P Vazquez, A G Schijman, A Panebra, et al.
Annales De Chirurgie Plastique Et Esthetique
|
May 24, 2016
[Electromyographic assessment of the temporalis muscle prior to a lengthening myoplasty in patients with Moebius syndrome]
F Renault, B Sergent, V Charpillet, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
April 1, 1996
Intraoral distraction for mandibular lengthening: a technical innovation
P A Diner, E M Kollar, H Martinez, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
November 20, 1998
Arteriovenous malformations of the dental arcades. The place of endovascular therapy: results in 12 cases are presented
G Rodesch, V Soupre, M P Vazquez, et al.
Revue De Stomatologie Et De Chirurgie Maxillo-Faciale
|
August 11, 2007
[Maxillary sequelae in cleft patients. Causes of maxillary hypoplasia and possible prevention]
H Bénateau, P-A Diner, E Soubeyrand, et al.
Annales De Chirurgie Plastique Et Esthetique
|
January 5, 2002
[Oto-mandibular dysplasias: genetics and nomenclature of syndromes]
L Burglen, V Soupre, P A Diner, et al.
Hormone Research
|
February 22, 2001
Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome
V Gaston, Y Le Bouc, V Soupre, et al.
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Search research articles
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Showing results (21-30 of 91) with videos related to
Sort By:
Page
of 10
Annales De Chirurgie Plastique Et Esthetique
|
September 6, 2001
[Mandibular advancement: osteotomy or distraction osteogenesis? A case report]
P A Diner, C Tomat, V Soupre, et al.
Growth Regulation
|
December 1, 1991
Loss of heterozygosity in non-tumoral tissue in two children with Beckwith-Wiedemann syndrome
H Schneid, M P Vazquez, D Seurin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 26, 2011
[Congenital epulis: refrain from surgery. A case report of spontaneous regression]
N Kadlub, E Galliani, N Oker, et al.
Nucleic Acids Research
|
June 11, 1992
Nucleotide sequence of a cDNA encoding another Trypanosoma cruzi acidic ribosomal P2 type protein (TcP2b)
M P Vazquez, A G Schijman, A Panebra, et al.
Annales De Chirurgie Plastique Et Esthetique
|
May 24, 2016
[Electromyographic assessment of the temporalis muscle prior to a lengthening myoplasty in patients with Moebius syndrome]
F Renault, B Sergent, V Charpillet, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
April 1, 1996
Intraoral distraction for mandibular lengthening: a technical innovation
P A Diner, E M Kollar, H Martinez, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
November 20, 1998
Arteriovenous malformations of the dental arcades. The place of endovascular therapy: results in 12 cases are presented
G Rodesch, V Soupre, M P Vazquez, et al.
Revue De Stomatologie Et De Chirurgie Maxillo-Faciale
|
August 11, 2007
[Maxillary sequelae in cleft patients. Causes of maxillary hypoplasia and possible prevention]
H Bénateau, P-A Diner, E Soubeyrand, et al.
Annales De Chirurgie Plastique Et Esthetique
|
January 5, 2002
[Oto-mandibular dysplasias: genetics and nomenclature of syndromes]
L Burglen, V Soupre, P A Diner, et al.
Hormone Research
|
February 22, 2001
Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome
V Gaston, Y Le Bouc, V Soupre, et al.
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of 10