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M Bitner-Glindzicz

Showing results (21-30 of 36) with videos related to

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Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Archives of Disease in Childhood|February 23, 2010
Aminoglycoside-induced deafness during treatment of acute leukaemiaM Bitner-Glindzicz, V Osei-Lah, I Colvin, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Clinical Genetics|November 15, 2005
Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testingT Hutchin, N N Coy, H Conlon, et al.
Human Molecular Genetics|August 1, 1995
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3M Bitner-Glindzicz, P Turnpenny, P Höglund, et al.
Clinical Genetics|September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlationsX Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
Human Molecular Genetics|July 1, 1994
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Archives of Disease in Childhood|February 23, 2010
Aminoglycoside-induced deafness during treatment of acute leukaemiaM Bitner-Glindzicz, V Osei-Lah, I Colvin, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Clinical Genetics|November 15, 2005
Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testingT Hutchin, N N Coy, H Conlon, et al.
Human Molecular Genetics|August 1, 1995
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3M Bitner-Glindzicz, P Turnpenny, P Höglund, et al.
Clinical Genetics|September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlationsX Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
Human Molecular Genetics|July 1, 1994
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Pageof 4