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Page 1
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome.
Gausden E, Armour JA, Coyle B, Coffey R, Hochberg Z, Pembrey M, Britton KE, Grossman A, Reardon W, Trembath R. Gausden E, et al. Among authors: pembrey m. Clin Endocrinol (Oxf). 1996 Apr;44(4):441-6. doi: 10.1046/j.1365-2265.1996.714536.x. Clin Endocrinol (Oxf). 1996. PMID: 8706311
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: pembrey me. 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: pembrey me. Clin Radiol. 1998 Apr;53(4):268-73. doi: 10.1016/s0009-9260(98)80125-6. Clin Radiol. 1998. PMID: 9585042
The genetics of deafness.
Reardon W, Pembrey M. Reardon W, et al. Among authors: pembrey m. Arch Dis Child. 1990 Nov;65(11):1196-7. doi: 10.1136/adc.65.11.1196. Arch Dis Child. 1990. PMID: 2248525 Free PMC article. No abstract available.
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. Among authors: pembrey me. Br J Audiol. 1992 Apr;26(2):109-14. doi: 10.3109/03005369209077878. Br J Audiol. 1992. PMID: 1628115
261 results