E. Gausden

Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome

M. Pembrey, W. Reardon, J. Armour, 1996, Clinical endocrinology.

Molecular analysis of the PDS gene in Pendred syndrome.

S. Scherer, L. Tsui, W. Reardon, 1998, Human molecular genetics.

Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage.

M. Pembrey, W. Reardon, R. Winter, 1997, Journal of medical genetics.

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

M. Pembrey, W. Reardon, J. Armour, 1996, Nature Genetics.