Showing results (41-50 of 51) with videos related to
Sort By:
Pageof 6
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.Neurology|April 1, 1995
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14K Bejaoui, K Hirabayashi, F Hentati, et al.La Tunisie Medicale|February 8, 2008
[Prognostic factors of pneumococcal meningitis. Retrospective study of 31 cases]H Kallel, I Mâaloul, F Mahjoubi, et al.La Tunisie Medicale|June 23, 2005
[Evaluation of the antibiotics consumption in a Tunisian university hospital]H Kallel, C Hedi, I Maaloul, et al.Gynecologie, Obstetrique & Fertilite|July 11, 2006
[Acute fatty liver of pregnancy. About 22 cases]M Bahloul, H Dammak, N Khlaf-Bouaziz, et al.Nature Genetics|July 1, 1994
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35A Hentati, K Bejaoui, M A Pericak-Vance, et al.Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.Nature Genetics|November 4, 2000
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathyP Bomont, L Cavalier, F Blondeau, et al.Nature Genetics|December 1, 1992
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13qK Ben Othmane, M Ben Hamida, M A Pericak-Vance, et al.Annales Francaises D'Anesthesie Et De Reanimation|December 30, 2008
[Peripartum cardiomyopathy: incidence, pathogenesis, diagnosis, treatment and prognosis]M Bahloul, M N Ben Ahmed, L Laaroussi, et al.Pageof 6