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Showing results (31-40 of 35) with videos related to

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Clinical Genetics|April 3, 2012
Phenotype in 18 Danish subjects with genetically verified CHARGE syndromeE Husu, H D Hove, S Farholt, et al.
Journal of Medical Genetics|May 2, 2006
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 geneH Eiberg, L Hansen, B Kjer, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|November 24, 2007
Streptococcus pneumoniae: proteomics of surface proteins for vaccine developmentC Morsczeck, T Prokhorova, J Sigh, et al.
Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.
B-ENT|January 30, 2008
Familial aggregation of tinnitus: a European multicentre studyJ J Hendrickx, J R Huyghe, K Demeester, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Clinical Genetics|April 3, 2012
Phenotype in 18 Danish subjects with genetically verified CHARGE syndromeE Husu, H D Hove, S Farholt, et al.
Journal of Medical Genetics|May 2, 2006
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 geneH Eiberg, L Hansen, B Kjer, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|November 24, 2007
Streptococcus pneumoniae: proteomics of surface proteins for vaccine developmentC Morsczeck, T Prokhorova, J Sigh, et al.
Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.
B-ENT|January 30, 2008
Familial aggregation of tinnitus: a European multicentre studyJ J Hendrickx, J R Huyghe, K Demeester, et al.
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