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S Abdelhak

Showing results (11-20 of 56) with videos related to

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Nucleic Acids Research|September 25, 1990
A PstI polymorphism at the D5S39 locusS Abdelhak, J Melki, M F Bachelot, et al.
Pathologie-Biologie|December 5, 2006
[Homozygous antithrombin type HBS deficiency; a family study]S Guermazi, H Elloumi-ZghaL, L Ben Hassine, et al.
Journal Francais D'Ophtalmologie|September 10, 2014
Retinal dystrophy and congenital glaucoma as major causes of vision loss in students attending two institutions for the visually disabled in Tunis city, TunisiaI Chouchene, K Derouiche, N Ben Halim, et al.
Cytogenetics and Cell Genetics|January 1, 1991
In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3M G Mattei, J Melki, M F Bachelot, et al.
Advances in Experimental Medicine and Biology|August 16, 2003
MICA transmembrane region polymorphism and HLA B51 in Tunisian Behçet's disease patientsM Ben Ahmed, H Houman, S Abdelhak, et al.
Pathologie-Biologie|November 10, 2009
[Biochemical and molecular diagnosis of primary hyperoxaluria type 1: Tunisian study about 15 cases]R Belhaj, N Hayder, T Gargueh, et al.
Advances in Nephrology From the Necker Hospital|January 16, 1999
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeJ P Hardelin, N Soussi-Yanicostas, J Levilliers, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
BOR and BO syndromes are allelic defects of EYA1C Vincent, V Kalatzis, S Abdelhak, et al.
Clinical Genetics|February 6, 2004
Heterozygous manifestations in female carriers of Mal de MeledaM Mokni, C Charfeddine, R Ben Mously, et al.
La Revue De Medecine Interne|August 7, 2002
[Neurologic manifestations of Behcet's disease: analysis of a series of 27 patients]M H Houman, S Hamzaoui-B'Chir, I Ben Ghorbel, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Nucleic Acids Research|September 25, 1990
A PstI polymorphism at the D5S39 locusS Abdelhak, J Melki, M F Bachelot, et al.
Pathologie-Biologie|December 5, 2006
[Homozygous antithrombin type HBS deficiency; a family study]S Guermazi, H Elloumi-ZghaL, L Ben Hassine, et al.
Journal Francais D'Ophtalmologie|September 10, 2014
Retinal dystrophy and congenital glaucoma as major causes of vision loss in students attending two institutions for the visually disabled in Tunis city, TunisiaI Chouchene, K Derouiche, N Ben Halim, et al.
Cytogenetics and Cell Genetics|January 1, 1991
In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3M G Mattei, J Melki, M F Bachelot, et al.
Advances in Experimental Medicine and Biology|August 16, 2003
MICA transmembrane region polymorphism and HLA B51 in Tunisian Behçet's disease patientsM Ben Ahmed, H Houman, S Abdelhak, et al.
Pathologie-Biologie|November 10, 2009
[Biochemical and molecular diagnosis of primary hyperoxaluria type 1: Tunisian study about 15 cases]R Belhaj, N Hayder, T Gargueh, et al.
Advances in Nephrology From the Necker Hospital|January 16, 1999
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeJ P Hardelin, N Soussi-Yanicostas, J Levilliers, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
BOR and BO syndromes are allelic defects of EYA1C Vincent, V Kalatzis, S Abdelhak, et al.
Clinical Genetics|February 6, 2004
Heterozygous manifestations in female carriers of Mal de MeledaM Mokni, C Charfeddine, R Ben Mously, et al.
La Revue De Medecine Interne|August 7, 2002
[Neurologic manifestations of Behcet's disease: analysis of a series of 27 patients]M H Houman, S Hamzaoui-B'Chir, I Ben Ghorbel, et al.
Pageof 6