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Annales De Biologie Clinique|November 28, 2007

[Biochemical and molecular diagnosis of Gaucher disease in Tunisia]A Dandana, S Ferchichi, S Khedhiri, 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.

Clinical Genetics|March 25, 2018

Single, short in-del, and copy number variations detection in monogenic dyslipidemia using a next-generation sequencing strategyO Marmontel, S Charrière, T Simonet, et al.

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Search research articles

Showing results (51-60 of 53) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 53 results.

Annales De Biologie Clinique|November 28, 2007

[Biochemical and molecular diagnosis of Gaucher disease in Tunisia]A Dandana, S Ferchichi, S Khedhiri, 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.

Clinical Genetics|March 25, 2018

Single, short in-del, and copy number variations detection in monogenic dyslipidemia using a next-generation sequencing strategyO Marmontel, S Charrière, T Simonet, et al.

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