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J C Lambert

Showing results (41-50 of 112) with videos related to

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Pediatrie|March 1, 1979
[4p monosomy with paternal t(13;14) (p11;p11) translocation]J C Lambert, J Rovinski, J F Mattei, et al.
The British Journal of Dermatology|April 8, 2021
Dupilumab-associated arthralgia: an observational retrospective study in VigiBase<sup>®</sup>B Chrétien, C Dolladille, J Alexandre, et al.
Journal Francais D'Ophtalmologie|February 9, 2007
[Glaucoma with aniridia and isolated congenital glaucoma in siblings: contribution and limits of genetics]B Lise-Schneider, P Calvas, O Roche, et al.
Pediatrie|October 1, 1986
[Problems posed by the association of hemophilia A and congenital adrenal hyperplasia caused by 21-hydroxylase deficiency]P Boutte, H Madar, M d'Ollone, et al.
Clinical Genetics|March 18, 2006
A novel homozygous MMP2 mutation in a family with Winchester syndromeC Rouzier, R Vanatka, S Bannwarth, et al.
Journal of Cell Science|February 22, 2000
Evidence for deterministic chaos in aperiodic oscillations of proliferative activity in long-term cultured Fao hepatoma cellsC Wolfrom, N P Chau, J Maigné, et al.
Neuroscience Letters|December 6, 1996
Analysis of the APOE alleles impact in Down's syndromeJ C Lambert, J Pérez-Tur, M J Dupire, et al.
Pediatrie|January 1, 1992
[Molecular biology in genetic counseling of Duchenne and Becker myopathy]N Philip, M A Voelckel, L Girardot, et al.
The Pharmacogenomics Journal|August 22, 2003
Relevance and limitations of public databases for microarray design: a critical approach to gene predictionsJ C Lambert, E Testa, V Cognat, et al.
In Vitro|June 1, 1983
Establishment, characterization, and response to cytotoxic and radiation treatment of three human melanoma cell linesA Courdi, J Gioanni, C M Lalanne, et al.
Pageof 12

Showing results (41-50 of 112) with videos related to

Sort By:
Pageof 12
Pediatrie|March 1, 1979
[4p monosomy with paternal t(13;14) (p11;p11) translocation]J C Lambert, J Rovinski, J F Mattei, et al.
The British Journal of Dermatology|April 8, 2021
Dupilumab-associated arthralgia: an observational retrospective study in VigiBase<sup>®</sup>B Chrétien, C Dolladille, J Alexandre, et al.
Journal Francais D'Ophtalmologie|February 9, 2007
[Glaucoma with aniridia and isolated congenital glaucoma in siblings: contribution and limits of genetics]B Lise-Schneider, P Calvas, O Roche, et al.
Pediatrie|October 1, 1986
[Problems posed by the association of hemophilia A and congenital adrenal hyperplasia caused by 21-hydroxylase deficiency]P Boutte, H Madar, M d'Ollone, et al.
Clinical Genetics|March 18, 2006
A novel homozygous MMP2 mutation in a family with Winchester syndromeC Rouzier, R Vanatka, S Bannwarth, et al.
Journal of Cell Science|February 22, 2000
Evidence for deterministic chaos in aperiodic oscillations of proliferative activity in long-term cultured Fao hepatoma cellsC Wolfrom, N P Chau, J Maigné, et al.
Neuroscience Letters|December 6, 1996
Analysis of the APOE alleles impact in Down's syndromeJ C Lambert, J Pérez-Tur, M J Dupire, et al.
Pediatrie|January 1, 1992
[Molecular biology in genetic counseling of Duchenne and Becker myopathy]N Philip, M A Voelckel, L Girardot, et al.
The Pharmacogenomics Journal|August 22, 2003
Relevance and limitations of public databases for microarray design: a critical approach to gene predictionsJ C Lambert, E Testa, V Cognat, et al.
In Vitro|June 1, 1983
Establishment, characterization, and response to cytotoxic and radiation treatment of three human melanoma cell linesA Courdi, J Gioanni, C M Lalanne, et al.
Pageof 12