Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.

Por White, L. M., Rogan, P. K., Nicholls, R. D., Wu, B. L., Korf, B., Knoll, J. H.
Publicado em 1996

Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines.

Por Shiloh, Y, Shipley, J, Brodeur, G M, Bruns, G, Korf, B, Donlon, T, Schreck, R R, Seeger, R, Sakai, K, Latt, S A
Publicado em 1985

Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations.

Por Paznekas, W A, Cunningham, M L, Howard, T D, Korf, B R, Lipson, M H, Grix, A W, Feingold, M, Goldberg, R, Borochowitz, Z, Aleck, K, Mulliken, J, Yin, M, Jabs, E W
Publicado em 1998

Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)

Por Seizinger, B. R., Farmer, G. E., Haines, J. L., Ozelius, L. J., Anderson, K., Korf, B. R., Parry, D. M., Pericak-Vance, M. A., Mulvihill, J. J., Menon, A., Hobbs, W. J., Martuza, R. L., Gusella, J. F.
Publicado em 1989