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