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M Chaabouni

Showing results (61-70 of 66) with videos related to

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Annales De Genetique|August 28, 2001
Prenatal diagnosis of chromosome disorders in Tunisian populationH Chaabouni, M Chaabouni, F Maazoul, et al.
La Revue De Medecine Interne|January 28, 2004
[Gaucher's disease in Tunisia (multicenter study)]M Chaabouni, H Aoulou, N Tebib, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 31, 2007
[Mucopolysaccharidosis type I: identification of alpha-L-iduronidase mutations in Tunisian families]L Chkioua, S Khedhiri, Z Jaidane, et al.
Annales De Biologie Clinique|March 14, 2007
[Diagnostic strategy of mucopolysaccharidosis type I in Tunisia]L Chkioua, S Ferchichi, S Khedhiri, et al.
Annales De Biologie Clinique|February 1, 2007
[Clinical, biologic and molecular characteristics of two Tunisian MPS IV A patients]S Khedhiri, L Chkioua, S Ferchichi, et al.
La Tunisie Medicale|March 26, 2002
[Diagnosis of holoprosencephalia. Report of 17 cases]S Siala Gaigi, A Masmoudi, M B Chennoufi, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
Annales De Genetique|August 28, 2001
Prenatal diagnosis of chromosome disorders in Tunisian populationH Chaabouni, M Chaabouni, F Maazoul, et al.
La Revue De Medecine Interne|January 28, 2004
[Gaucher's disease in Tunisia (multicenter study)]M Chaabouni, H Aoulou, N Tebib, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 31, 2007
[Mucopolysaccharidosis type I: identification of alpha-L-iduronidase mutations in Tunisian families]L Chkioua, S Khedhiri, Z Jaidane, et al.
Annales De Biologie Clinique|March 14, 2007
[Diagnostic strategy of mucopolysaccharidosis type I in Tunisia]L Chkioua, S Ferchichi, S Khedhiri, et al.
Annales De Biologie Clinique|February 1, 2007
[Clinical, biologic and molecular characteristics of two Tunisian MPS IV A patients]S Khedhiri, L Chkioua, S Ferchichi, et al.
La Tunisie Medicale|March 26, 2002
[Diagnosis of holoprosencephalia. Report of 17 cases]S Siala Gaigi, A Masmoudi, M B Chennoufi, et al.
Pageof 7