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Human Molecular Genetics|December 1, 1996
Mapping of DFN2 to Xq22J Tyson, S Bellman, V Newton, et al.Current Opinion in Genetics & Development|June 1, 1995
Mapping and cloning hereditary deafness genesF P Cremers, M Bitner-Glindzicz, M E Pembrey, et al.American Journal of Medical Genetics|March 7, 2000
Jervell and Lange-Nielsen syndrome: a Norwegian perspectiveL Tranebjaerg, J Bathen, J Tyson, 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.Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.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|January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndromeB B de Vries, M Bitner-Glindzicz, S J Knight, 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.Journal of Medical Genetics|April 3, 2001
Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairmentT P Hutchin, K R Thompson, M Parker, 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.Pageof 96