Authors: Noll, WW Belloni, DR Rutter, JL Storm, CA Schned, AR Titus-Ernstoff, L Ernstoff, MS Brinckerhoff, CE

Citation: Ww. Noll et al., Loss of heterozygosity on chromosome 11q22-23 in melanoma is associated with retention of the insertion polymorphism in the matrix metalloproteinase-1 promoter, AM J PATH, 158(2), 2001, pp. 691-697

Authors: Noll, WW Belloni, DR Stenzel, TT Grody, WW

Citation: Ww. Noll et al., Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results, NAT GENET, 23(3), 1999, pp. 271-272

Authors: Mohandas, TK Park, JP Spellman, RA Filiano, JJ Mamourian, AC Hawk, AB Belloni, DR Noll, WW Moeschler, JB

Citation: Tk. Mohandas et al., Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay, AM J MED G, 82(4), 1999, pp. 294-300