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Pendred syndrome--100 years of underascertainment?
Reardon W, Coffey R, Phelps PD, Luxon LM, Stephens D, Kendall-Taylor P, Britton KE, Grossman A, Trembath R. Reardon W, et al. Among authors: luxon lm. QJM. 1997 Jul;90(7):443-7. doi: 10.1093/qjmed/90.7.443. QJM. 1997. PMID: 9302427
Molecular analysis of the PDS gene in Pendred syndrome.
Coyle B, Reardon W, Herbrick JA, Tsui LC, Gausden E, Lee J, Coffey R, Grueters A, Grossman4 A, Phelps PD, Luxon L, Kendall-Taylor P, Scherer SW, Trembath RC. Coyle B, et al. Hum Mol Genet. 1998 Jul;7(7):1105-12. doi: 10.1093/hmg/7.7.1105. Hum Mol Genet. 1998. PMID: 9618167
Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage.
Gausden E, Coyle B, Armour JA, Coffey R, Grossman A, Fraser GR, Winter RM, Pembrey ME, Kendall-Taylor P, Stephens D, Luxon LM, Phelps PD, Reardon W, Trembath R. Gausden E, et al. Among authors: luxon lm. J Med Genet. 1997 Feb;34(2):126-9. doi: 10.1136/jmg.34.2.126. J Med Genet. 1997. PMID: 9039988 Free PMC article.
Radiological malformations of the ear in Pendred syndrome.
Phelps PD, Coffey RA, Trembath RC, Luxon LM, Grossman AB, Britton KE, Kendall-Taylor P, Graham JM, Cadge BC, Stephens SG, Pembrey ME, Reardon W. Phelps PD, et al. Among authors: luxon lm. Clin Radiol. 1998 Apr;53(4):268-73. doi: 10.1016/s0009-9260(98)80125-6. Clin Radiol. 1998. PMID: 9585042
Neuro-otological findings in Pendred syndrome.
Luxon LM, Cohen M, Coffey RA, Phelps PD, Britton KE, Jan H, Trembath RC, Reardon W. Luxon LM, et al. Int J Audiol. 2003 Mar;42(2):82-8. doi: 10.3109/14992020309078339. Int J Audiol. 2003. PMID: 12641391
Clinical and genetic heterogeneity in X-linked deafness.
Reardon W, Middleton-Price HR, Malcolm S, Phelps P, Bellman S, Luxon L, Martin JA, Bumby A, Pembrey ME. Reardon W, et al. Br J Audiol. 1992 Apr;26(2):109-14. doi: 10.3109/03005369209077878. Br J Audiol. 1992. PMID: 1628115
118 results