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V El Ghouzzi

Showing results (1-10 of 12) with videos related to

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Journal of Neurosurgery|April 13, 2000
Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcomeD Renier, V El-Ghouzzi, J Bonaventure, et al.
Journal of Medical Genetics|February 9, 1999
Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutationE Lajeunie, V El Ghouzzi, M Le Merrer, et al.
Journal of Neurosurgery|November 13, 2001
Craniosynostosis and fetal exposure to sodium valproateE Lajeunie, U Barcik, J A Thorne, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndromeV El Ghouzzi, E Lajeunie, M Le Merrer, et al.
Human Molecular Genetics|April 6, 2000
Saethre-Chotzen mutations cause TWIST protein degradation or impaired nuclear locationV El Ghouzzi, L Legeai-Mallet, S Aresta, et al.
Clinical Dysmorphology|October 25, 2000
Overlap between Baller-Gerold and Rothmund-Thomson syndromeA Mégarbané, I Melki, N Souraty, et al.
Cellular and Molecular Life Sciences : CMLS|September 7, 2005
Succinate dehydrogenase deficiency in humanJ-J Brière, J Favier, V El Ghouzzi, et al.
FEBS Letters|March 15, 2001
Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndromeV El Ghouzzi, L Legeai-Mallet, C Benoist-Lasselin, et al.
Human Molecular Genetics|April 1, 1996
Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1)F Rousseau, V el Ghouzzi, A L Delezoide, et al.
Journal of Neurosurgery|March 6, 1999
Clinical variability in patients with Apert's syndromeE Lajeunie, R Cameron, V El Ghouzzi, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Neurosurgery|April 13, 2000
Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcomeD Renier, V El-Ghouzzi, J Bonaventure, et al.
Journal of Medical Genetics|February 9, 1999
Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutationE Lajeunie, V El Ghouzzi, M Le Merrer, et al.
Journal of Neurosurgery|November 13, 2001
Craniosynostosis and fetal exposure to sodium valproateE Lajeunie, U Barcik, J A Thorne, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndromeV El Ghouzzi, E Lajeunie, M Le Merrer, et al.
Human Molecular Genetics|April 6, 2000
Saethre-Chotzen mutations cause TWIST protein degradation or impaired nuclear locationV El Ghouzzi, L Legeai-Mallet, S Aresta, et al.
Clinical Dysmorphology|October 25, 2000
Overlap between Baller-Gerold and Rothmund-Thomson syndromeA Mégarbané, I Melki, N Souraty, et al.
Cellular and Molecular Life Sciences : CMLS|September 7, 2005
Succinate dehydrogenase deficiency in humanJ-J Brière, J Favier, V El Ghouzzi, et al.
FEBS Letters|March 15, 2001
Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndromeV El Ghouzzi, L Legeai-Mallet, C Benoist-Lasselin, et al.
Human Molecular Genetics|April 1, 1996
Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1)F Rousseau, V el Ghouzzi, A L Delezoide, et al.
Journal of Neurosurgery|March 6, 1999
Clinical variability in patients with Apert's syndromeE Lajeunie, R Cameron, V El Ghouzzi, et al.
Pageof 2