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J Bonaventure

Showing results (11-20 of 81) with videos related to

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Archives Francaises De Pediatrie|April 1, 1986
[Antenatal forms of osteogenesis imperfecta. Classification trial]P Maroteaux, J Frézal, L Cohen-Solal, et al.
Human Genetics|August 1, 1992
A dominant mutation in the COL1A1 gene that substitutes glycine for valine causes recurrent lethal osteogenesis imperfectaJ Bonaventure, L Cohen-Solal, C Lasselin, et al.
Annales D'Endocrinologie|January 1, 1996
[Association of achondroplasia to a mutation in the transmembrane domain of fibroblastic growth factor receptor 3 (FGFR3)]F Rousseau, J Bonaventure, M Le Merrer, et al.
American Journal of Medical Genetics|May 3, 1996
Dyssegmental dysplasia with glaucomaP Maroteaux, S Manouvrier, J Bonaventure, et al.
Canadian Journal of Anaesthesia = Journal Canadien D'Anesthesie|March 20, 2009
Tetanus in developing countries: a case series and reviewKara Gibson, J Bonaventure Uwineza, Willy Kiviri, et al.
British Journal of Cancer|November 1, 1982
Effects of structural variations in synthetic glycolipids upon mitogenicity for spleen lymphocytes, adjuvancy for humoral immune response and on anti-tumour potentialV N Nigam, J Bonaventure, C Chopra, et al.
Bone|January 31, 2004
Overexpression of FGFR3, Stat1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasiasL Legeai-Mallet, C Benoist-Lasselin, A Munnich, et al.
American Journal of Medical Genetics|April 5, 2000
Monozygotic twins with Crouzon syndrome: concordance for craniosynostosis and discordance for thumb duplicationE Lajeunie, J Bonaventure, V El Ghouzzi, et al.
Journal of Medical Genetics|July 1, 1992
Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndromeJ Bonaventure, C Lasselin, J Mellier, et al.
Annales D'Endocrinologie|January 1, 1996
[Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia]F Rousseau, J Bonaventure, M Le Merrer, et al.
Pageof 9

Showing results (11-20 of 81) with videos related to

Sort By:
Pageof 9
Archives Francaises De Pediatrie|April 1, 1986
[Antenatal forms of osteogenesis imperfecta. Classification trial]P Maroteaux, J Frézal, L Cohen-Solal, et al.
Human Genetics|August 1, 1992
A dominant mutation in the COL1A1 gene that substitutes glycine for valine causes recurrent lethal osteogenesis imperfectaJ Bonaventure, L Cohen-Solal, C Lasselin, et al.
Annales D'Endocrinologie|January 1, 1996
[Association of achondroplasia to a mutation in the transmembrane domain of fibroblastic growth factor receptor 3 (FGFR3)]F Rousseau, J Bonaventure, M Le Merrer, et al.
American Journal of Medical Genetics|May 3, 1996
Dyssegmental dysplasia with glaucomaP Maroteaux, S Manouvrier, J Bonaventure, et al.
Canadian Journal of Anaesthesia = Journal Canadien D'Anesthesie|March 20, 2009
Tetanus in developing countries: a case series and reviewKara Gibson, J Bonaventure Uwineza, Willy Kiviri, et al.
British Journal of Cancer|November 1, 1982
Effects of structural variations in synthetic glycolipids upon mitogenicity for spleen lymphocytes, adjuvancy for humoral immune response and on anti-tumour potentialV N Nigam, J Bonaventure, C Chopra, et al.
Bone|January 31, 2004
Overexpression of FGFR3, Stat1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasiasL Legeai-Mallet, C Benoist-Lasselin, A Munnich, et al.
American Journal of Medical Genetics|April 5, 2000
Monozygotic twins with Crouzon syndrome: concordance for craniosynostosis and discordance for thumb duplicationE Lajeunie, J Bonaventure, V El Ghouzzi, et al.
Journal of Medical Genetics|July 1, 1992
Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndromeJ Bonaventure, C Lasselin, J Mellier, et al.
Annales D'Endocrinologie|January 1, 1996
[Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia]F Rousseau, J Bonaventure, M Le Merrer, et al.
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