F. Bullrich

Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa.

J. Uitto, F. Bullrich, L. Weiss, 1997, American journal of human genetics.

Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization.

E. Lane, R. Ray, S. DeArmond, 1996, Genes & development.

A novel zinc finger gene is fused to EWS in small round cell tumor

C. Croce, P. Radice, G. Sozzi, 2000, Oncogene.

Emergence of flat cells from glia in stationary cultures of embryonic chick neural retina

J. Sheffield, F. Bullrich, M. Moyer, 1990, In Vitro Cellular & Developmental Biology.