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Pediatrie
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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 syndrome
C 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 cells
C Wolfrom, N P Chau, J Maigné, et al.
Neuroscience Letters
|
December 6, 1996
Analysis of the APOE alleles impact in Down's syndrome
J 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 predictions
J 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 lines
A Courdi, J Gioanni, C M Lalanne, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 112) with videos related to
Sort By:
Page
of 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 syndrome
C 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 cells
C Wolfrom, N P Chau, J Maigné, et al.
Neuroscience Letters
|
December 6, 1996
Analysis of the APOE alleles impact in Down's syndrome
J 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 predictions
J 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 lines
A Courdi, J Gioanni, C M Lalanne, et al.
Page
of 12