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La Tunisie Medicale
|
April 1, 1993
[Renal anthrax: a case report in a child]
A Mahfoudh, N Mattoussi, A Karray, et al.
Clinical Genetics
|
March 19, 2010
FOXL2 mutations in Tunisian patients with blepharophimosis-ptosis-epicanthus inversus syndrome
L Kraoua, M Chaabouni, M Trabelsi, et al.
Annales D'Endocrinologie
|
June 11, 2008
[Genetic analysis of Turner syndrome: 89 cases in Tunisia]
I Kammoun, M Chaabouni, M Trabelsi, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Mucopolysaccharidosis I: Alpha-L-Iduronidase mutations in three Tunisian families
S Laradi, T Tukel, M Erazo, et al.
Molecular Genetics and Metabolism
|
December 28, 2005
Mucopolysaccharidosis type IV: N-acetylgalactosamine-6-sulfatase mutations in Tunisian patients
S Laradi, T Tukel, S Khediri, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 18, 2016
Burkitt lymphoma in a child with Bloom syndrome
F Fedhila-Ben Ayed, W Douira-Khomsi, S Rhayem, et al.
Clinical Genetics
|
March 25, 2010
Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V
M Kharrat, S Trabelsi, M Chaabouni, et al.
Clinical Genetics
|
February 26, 2013
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis
O M'hamdi, C Redin, C Stoetzel, et al.
Journal Francais D'Ophtalmologie
|
June 25, 2005
[Retinal detachment after Excimer laser (myopic LASIK or PRK). A retrospective multicentric study: 15 cases]
J Feki, A Trigui, M Chaabouni, et al.
La Tunisie Medicale
|
August 23, 2001
[Mucopolysaccharidoses in children. Experience of a general pediatric service. 11 cases]
M Chaabouni, M Ben Slimen, M Boudawara, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 66) with videos related to
Sort By:
Page
of 7
La Tunisie Medicale
|
April 1, 1993
[Renal anthrax: a case report in a child]
A Mahfoudh, N Mattoussi, A Karray, et al.
Clinical Genetics
|
March 19, 2010
FOXL2 mutations in Tunisian patients with blepharophimosis-ptosis-epicanthus inversus syndrome
L Kraoua, M Chaabouni, M Trabelsi, et al.
Annales D'Endocrinologie
|
June 11, 2008
[Genetic analysis of Turner syndrome: 89 cases in Tunisia]
I Kammoun, M Chaabouni, M Trabelsi, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Mucopolysaccharidosis I: Alpha-L-Iduronidase mutations in three Tunisian families
S Laradi, T Tukel, M Erazo, et al.
Molecular Genetics and Metabolism
|
December 28, 2005
Mucopolysaccharidosis type IV: N-acetylgalactosamine-6-sulfatase mutations in Tunisian patients
S Laradi, T Tukel, S Khediri, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 18, 2016
Burkitt lymphoma in a child with Bloom syndrome
F Fedhila-Ben Ayed, W Douira-Khomsi, S Rhayem, et al.
Clinical Genetics
|
March 25, 2010
Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V
M Kharrat, S Trabelsi, M Chaabouni, et al.
Clinical Genetics
|
February 26, 2013
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis
O M'hamdi, C Redin, C Stoetzel, et al.
Journal Francais D'Ophtalmologie
|
June 25, 2005
[Retinal detachment after Excimer laser (myopic LASIK or PRK). A retrospective multicentric study: 15 cases]
J Feki, A Trigui, M Chaabouni, et al.
La Tunisie Medicale
|
August 23, 2001
[Mucopolysaccharidoses in children. Experience of a general pediatric service. 11 cases]
M Chaabouni, M Ben Slimen, M Boudawara, et al.
Page
of 7