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: Park, JP Ladd, SL Fly, P Weiner, NJ Wojiski, SA Hawk, AB Noll, WW Mohandas, TK

Citation: Jp. Park et al., Amplification of the MLL region in acute myeloid leukemia, CANC GENET, 121(2), 2000, pp. 198-205

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

Authors: Grizzle, W Grody, WW Noll, WW Sobel, ME Stass, SA Trainer, T Travers, H Weedn, V Woodruff, K

Citation: W. Grizzle et al., Recommended policies for uses of human tissue in research, education, and quality control, ARCH PATH L, 123(4), 1999, pp. 296-300

Authors: Noll, WW

Citation: Ww. Noll, Utility of RET mutation analysis in multiple endocrine neoplasia type 2, ARCH PATH L, 123(11), 1999, pp. 1047-1049