T Rosenberg

Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1.

R. Reinhardt, A. Beck, R. Roepman, 1996, Human molecular genetics.

Identification of a novel locus for a USH3 like syndrome combined with congenital cataract

T. Thykjær, T. Rosenberg, T Rosenberg, 2010, Clinical genetics.

Clustering of mutations associated with mild Marfan-like phenotypes in the 3' region of FBN1 suggests a potential genotype-phenotype correlation.

P. Robinson, T. Rosenberg, C. Nienaber, 2000, American journal of medical genetics.

Prevalence of retinitis pigmentosa and allied disorders in Denmark

T. Rosenberg, N. Holm, N V Holm, 1992, Acta ophthalmologica.

A common ancestral origin of the frequent and widespread 2299delG USH2A mutation.

W J Kimberling, T Rosenberg, M D Weston, 2001, American journal of human genetics.

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

M Jay, N. Tommerup, E. Bruford, 1997, Genomics.