A. Sand

Population-based risk estimates of Wilms tumor in sporadic aniridia

J. Olsen, T. Rosenberg, K. Brøndum‐Nielsen, 2001, Human Genetics.

Birth prevalence and mutation spectrum in danish patients with autosomal recessive albinism.

T. Rosenberg, K. Brøndum‐Nielsen, K. Brixen, 2009, Investigative ophthalmology & visual science.

Mutational analysis of PAX6: 16 novel mutations including 5 missense mutations with a mild aniridia phenotype

T. Rosenberg, K. Brøndum‐Nielsen, K. Grønskov, 1999, European Journal of Human Genetics.

Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms

N. Tommerup, K. Brøndum‐Nielsen, M. Petersen, 1996, Human Genetics.

Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness

K. Brøndum‐Nielsen, A. Pampanos, K. Grønskov, 2000, Human mutation.

Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.

M. B. Peterson, A. Chakravarti, S. Antonarakis, 1992, American journal of human genetics.