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International Journal of Audiology|March 19, 2003
Neuro-otological findings in Pendred syndromeL M Luxon, M Cohen, R A Coffey, et al.Nature Genetics|April 1, 1996
Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4B Coyle, R Coffey, J A Armour, et al.Clinical Endocrinology|April 1, 1996
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndromeE Gausden, J A Armour, B Coyle, et al.American Journal of Medical Genetics|October 1, 1993
Mesomelic limb shortness: a previously unreported autosomal recessive typeW Reardon, C M Hall, S Slaney, et al.Human Molecular Genetics|August 1, 1994
Localization of the genetic locus for Saethre-Chotzen syndrome to a 6 cM region of chromosome 7 using four cases with apparently balanced translocations at 7p21.2C S Rose, A A King, D Summers, et al.QJM : Monthly Journal of the Association of Physicians|July 1, 1997
Pendred syndrome--100 years of underascertainment?W Reardon, R Coffey, P D Phelps, et al.British Journal of Audiology|April 1, 1992
Clinical and genetic heterogeneity in X-linked deafnessW Reardon, H R Middleton-Price, S Malcolm, et al.American Journal of Medical Genetics. Part A|February 12, 2009
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutationC P Barnett, R Mendoza-Londono, S Blaser, 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.American Journal of Human Genetics|January 23, 1999
Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypesM Tassabehji, K Metcalfe, A Karmiloff-Smith, et al.Pageof 16