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R J H Smith

Showing results (1-10 of 25) with videos related to

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Clinical Otolaryngology and Allied Sciences|July 23, 2003
Genetic screening for hearing lossS W Hone, R J H Smith
Clinical Genetics|July 31, 2007
Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigreeN C Meyer, C J Nishimura, S McMordie, et al.
Clinical Genetics|May 8, 2010
A novel mutation adjacent to the Bth mouse mutation in the TMC1 gene makes this mouse an excellent model of human deafness at the DFNA36 locusT Yang, K Kahrizi, N Bazazzadeghan, et al.
Kidney International|April 6, 2007
Mesangial immune complex glomerulonephritis due to complement factor D deficiencyM A Abrera-Abeleda, Y Xu, M C Pickering, et al.
AJNR. American Journal of Neuroradiology|May 29, 2009
The rare third branchial cleft cystM J Joshi, M J Provenzano, R J H Smith, et al.
Journal of Medical Genetics|April 10, 2009
A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian familyN Hilgert, K Kahrizi, N Dieltjens, et al.
Journal of Medical Genetics|July 22, 2005
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locusW Chen, K Kahrizi, N C Meyer, et al.
Clinical Genetics|May 11, 2007
Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosisW Chen, N C Meyer, M J McKenna, et al.
Clinical Genetics|May 21, 2004
The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish populationN Mahdieh, C Nishimura, K Ali-Madadi, 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.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Clinical Otolaryngology and Allied Sciences|July 23, 2003
Genetic screening for hearing lossS W Hone, R J H Smith
Clinical Genetics|July 31, 2007
Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigreeN C Meyer, C J Nishimura, S McMordie, et al.
Clinical Genetics|May 8, 2010
A novel mutation adjacent to the Bth mouse mutation in the TMC1 gene makes this mouse an excellent model of human deafness at the DFNA36 locusT Yang, K Kahrizi, N Bazazzadeghan, et al.
Kidney International|April 6, 2007
Mesangial immune complex glomerulonephritis due to complement factor D deficiencyM A Abrera-Abeleda, Y Xu, M C Pickering, et al.
AJNR. American Journal of Neuroradiology|May 29, 2009
The rare third branchial cleft cystM J Joshi, M J Provenzano, R J H Smith, et al.
Journal of Medical Genetics|April 10, 2009
A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian familyN Hilgert, K Kahrizi, N Dieltjens, et al.
Journal of Medical Genetics|July 22, 2005
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locusW Chen, K Kahrizi, N C Meyer, et al.
Clinical Genetics|May 11, 2007
Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosisW Chen, N C Meyer, M J McKenna, et al.
Clinical Genetics|May 21, 2004
The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish populationN Mahdieh, C Nishimura, K Ali-Madadi, 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.
Pageof 3