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G van Camp

Showing results (141-150 of 214) with videos related to

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The Quarterly Journal of Nuclear Medicine and Molecular Imaging : Official Publication of the Italian Association of Nuclear Medicine (AIMN) [And] the International Association of Radiopharmacology (IAR), [And] Section of the Society Of|March 21, 2007
In vivo visualization of 111In labeled CD133+ peripheral blood stem cells after intracoronary administration in patients with chronic ischemic heart diseaseV Caveliers, G De Keulenaer, H Everaert, et al.
Genetic Testing|February 24, 2001
The M34T allele variant of connexin 26R A Cucci, S Prasad, P M Kelley, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain geneK Kastury, W E Taylor, R Shen, et al.
The American Journal of Otology|November 27, 1998
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing lossP J Govaerts, G De Ceulaer, K Daemers, et al.
B-ENT|January 30, 2008
Prevalence of tinnitus and audiometric shapeK Demeester, A van Wieringen, J J Hendrickx, et al.
Archives of Otolaryngology--Head & Neck Surgery|January 24, 1998
Presymptomatic diagnosis of nonsyndromic hearing loss by genotypingA H Chen, R F Mueller, S D Prasad, et al.
American Journal of Human Genetics|April 16, 1998
Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21W Van Hul, W Balemans, E Van Hul, et al.
Journal of Medical Genetics|January 20, 2004
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3R L Snoeckx, H Kremer, R J H Ensink, et al.
Journal of Medical Genetics|June 3, 2004
DFNA5: hearing impairment exon instead of hearing impairment gene?L Van Laer, K Vrijens, S Thys, et al.
Archives of Otolaryngology--Head & Neck Surgery|August 26, 1998
Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472R J Ensink, K Verhoeven, H A Marres, et al.
Pageof 22

Showing results (141-150 of 214) with videos related to

Sort By:
Pageof 22
The Quarterly Journal of Nuclear Medicine and Molecular Imaging : Official Publication of the Italian Association of Nuclear Medicine (AIMN) [And] the International Association of Radiopharmacology (IAR), [And] Section of the Society Of|March 21, 2007
In vivo visualization of 111In labeled CD133+ peripheral blood stem cells after intracoronary administration in patients with chronic ischemic heart diseaseV Caveliers, G De Keulenaer, H Everaert, et al.
Genetic Testing|February 24, 2001
The M34T allele variant of connexin 26R A Cucci, S Prasad, P M Kelley, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain geneK Kastury, W E Taylor, R Shen, et al.
The American Journal of Otology|November 27, 1998
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing lossP J Govaerts, G De Ceulaer, K Daemers, et al.
B-ENT|January 30, 2008
Prevalence of tinnitus and audiometric shapeK Demeester, A van Wieringen, J J Hendrickx, et al.
Archives of Otolaryngology--Head & Neck Surgery|January 24, 1998
Presymptomatic diagnosis of nonsyndromic hearing loss by genotypingA H Chen, R F Mueller, S D Prasad, et al.
American Journal of Human Genetics|April 16, 1998
Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21W Van Hul, W Balemans, E Van Hul, et al.
Journal of Medical Genetics|January 20, 2004
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3R L Snoeckx, H Kremer, R J H Ensink, et al.
Journal of Medical Genetics|June 3, 2004
DFNA5: hearing impairment exon instead of hearing impairment gene?L Van Laer, K Vrijens, S Thys, et al.
Archives of Otolaryngology--Head & Neck Surgery|August 26, 1998
Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472R J Ensink, K Verhoeven, H A Marres, et al.
Pageof 22