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G Baujat

Showing results (21-30 of 35) with videos related to

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Pathologie-Biologie|February 6, 2004
[Rotavirus nosocomial infection in pediatric units. A multicentric observation study]I Sermet-Gaudelus, F de La Rocque, J-L Salomon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 29, 2014
[GACI syndrome: a case report with a neonatal beginning]C Freychet, C Gay, M-P Lavocat, et al.
Clinical Genetics|May 8, 2010
Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneityC Jung, N Dagoneau, G Baujat, et al.
Clinical Genetics|June 8, 2012
Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locusS K Holman, T Morgan, G Baujat, et al.
European Journal of Endocrinology|February 19, 2014
Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patientsI Flechtner, K Lambot-Juhan, R Teissier, et al.
Clinical Genetics|June 22, 2018
IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differencesE Brischoux-Boucher, A Trimouille, G Baujat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 14, 2012
[Prenatal symptoms and diagnosis of inherited metabolic diseases]A Brassier, C Ottolenghi, N Boddaert, et al.
European Journal of Endocrinology|March 26, 2014
Characterization and prevalence of severe primary IGF1 deficiency in a large cohort of French children with short statureR Teissier, I Flechtner, A Colmenares, et al.
Annales De Chirurgie Plastique Et Esthetique|October 4, 2016
[Craniofacial strategy for syndromic craniosynostosis]E Arnaud, G Paternoster, S James, et al.
Clinical Genetics|June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new familiesF Petit, A-S Jourdain, J Andrieux, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Pathologie-Biologie|February 6, 2004
[Rotavirus nosocomial infection in pediatric units. A multicentric observation study]I Sermet-Gaudelus, F de La Rocque, J-L Salomon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 29, 2014
[GACI syndrome: a case report with a neonatal beginning]C Freychet, C Gay, M-P Lavocat, et al.
Clinical Genetics|May 8, 2010
Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneityC Jung, N Dagoneau, G Baujat, et al.
Clinical Genetics|June 8, 2012
Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locusS K Holman, T Morgan, G Baujat, et al.
European Journal of Endocrinology|February 19, 2014
Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patientsI Flechtner, K Lambot-Juhan, R Teissier, et al.
Clinical Genetics|June 22, 2018
IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differencesE Brischoux-Boucher, A Trimouille, G Baujat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 14, 2012
[Prenatal symptoms and diagnosis of inherited metabolic diseases]A Brassier, C Ottolenghi, N Boddaert, et al.
European Journal of Endocrinology|March 26, 2014
Characterization and prevalence of severe primary IGF1 deficiency in a large cohort of French children with short statureR Teissier, I Flechtner, A Colmenares, et al.
Annales De Chirurgie Plastique Et Esthetique|October 4, 2016
[Craniofacial strategy for syndromic craniosynostosis]E Arnaud, G Paternoster, S James, et al.
Clinical Genetics|June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new familiesF Petit, A-S Jourdain, J Andrieux, et al.
Pageof 4