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Results: 4

Authors: COYLE B REARDON W HERBRICK JA TSUI LC GAUSDEN E LEE J COFFEY R GRUETERS A GROSSMAN A PHELPS PD LUXON L KENDALLTAYLOR P SCHERER SW TREMBATH RC
Citation: B. Coyle et al., MOLECULAR ANALYSIS OF THE PDS GENE IN PENDRED-SYNDROME (SENSORINEURALHEARING-LOSS AND GOITER), Human molecular genetics (Print), 7(7), 1998, pp. 1105-1112

Authors: GAUSDEN E COYLE B ARMOUR JAL COFFEY R GROSSMAN A FRASER GR WINTER RM PEMBREY ME KENDALLTAYLOR P STEPHENS D LUXON LM PHELPS PD REARDON W TREMBATH R
Citation: E. Gausden et al., PENDRED SYNDROME - EVIDENCE FOR GENETIC HOMOGENEITY AND FURTHER REFINEMENT OF LINKAGE, Journal of Medical Genetics, 34(2), 1997, pp. 126-129

Authors: COYLE B COFFEY R ARMOUR JAL GAUSDEN E HOCHBERG Z GROSSMAN A BRITTON K PEMBREY M REARDON W TREMBATH R
Citation: B. Coyle et al., PENDRED SYNDROME (GOITER AND SENSORINEURAL HEARING-LOSS) MAPS TO CHROMOSOME-7 IN THE REGION CONTAINING THE NONSYNDROMIC DEAFNESS GENE DFNB4, Nature genetics, 12(4), 1996, pp. 421-423

Authors: GAUSDEN E ARMOUR JAL COYLE B COFFEY R HOCHBERG Z PEMBREY M BRITTON KE GROSSMAN A REARDON W TREMBATH R
Citation: E. Gausden et al., THYROID PEROXIDASE - EVIDENCE FOR DISEASE GENE EXCLUSION IN PENDREDS-SYNDROME, Clinical endocrinology, 44(4), 1996, pp. 441-446
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