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Medecine Et Maladies Infectieuses
|
July 24, 2010
[Kawasaki disease and Mycoplasma pneumoniae infection]
J Chemli, S Hassayoun, S Ketata, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 6, 2014
[A rare cause of recurrent meningitis in children: cochleovestibular dysplasia]
H Ajmi, I Lahmar, N Zouari, et al.
Pathologie-Biologie
|
November 10, 2009
Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie
W Cherif, F Ben Rhouma, A Ben Chehida, et al.
Pathologie-Biologie
|
May 1, 2012
[Molecular diagnosis of Gaucher disease in Tunisia]
W Cherif, H Ben Turkia, F Ben Rhouma, et al.
Journal of Human Genetics
|
August 29, 2006
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia
R El Kares, M R Barbouche, H Elloumi-Zghal, et al.
Journal of Inherited Metabolic Disease
|
November 17, 2007
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis
E Barkaoui, W Cherif, N Tebib, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Medecine Et Maladies Infectieuses
|
July 24, 2010
[Kawasaki disease and Mycoplasma pneumoniae infection]
J Chemli, S Hassayoun, S Ketata, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 6, 2014
[A rare cause of recurrent meningitis in children: cochleovestibular dysplasia]
H Ajmi, I Lahmar, N Zouari, et al.
Pathologie-Biologie
|
November 10, 2009
Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie
W Cherif, F Ben Rhouma, A Ben Chehida, et al.
Pathologie-Biologie
|
May 1, 2012
[Molecular diagnosis of Gaucher disease in Tunisia]
W Cherif, H Ben Turkia, F Ben Rhouma, et al.
Journal of Human Genetics
|
August 29, 2006
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia
R El Kares, M R Barbouche, H Elloumi-Zghal, et al.
Journal of Inherited Metabolic Disease
|
November 17, 2007
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis
E Barkaoui, W Cherif, N Tebib, et al.
Page
of 2