Walter E. Nance

Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.

M. Tekin, K. Arnos, A. Pandya, 2001, Human molecular genetics.

Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: growth, development, and profiles.

A. Pandya, G. Fisch, W. Nance, 1999, American journal of medical genetics.

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12

A. Pandya, S. Blanton, D. Yan, 2005, Journal of Medical Genetics.

Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

K. Arnos, L. Farrer, C. Baldwin, 1994, American journal of human genetics.

Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNASer(UCN) in sensorineural hearing loss

A. Madeo, Walter E. Nance, Penelope L. Friedman, 2007, Clinical genetics.

Age-related language characteristics of children and adolescents with fragile X syndrome.

A. Pandya, G. Fisch, W. Nance, 1999, American journal of medical genetics.

Waardenburg syndrome type 3 (Klein–Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain of PAX3: a simple variant or a true syndrome?

M. Tekin, A. Pandya, W. Nance, 2001, Clinical genetics.