Authors: Barker, DF Denison, JC Atkin, CL Gregory, MC

Citation: Df. Barker et al., Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP, AM J MED G, 98(2), 2001, pp. 148-160

Authors: Heath, KE Campos-Barros, A Toren, A Rozenfeld-Granot, G Carlsson, LE Savige, J Denison, JC Gregory, MC White, JG Barker, DF Greinacher, A Epstein, CJ Glucksman, MJ Martignetti, JA

Citation: Ke. Heath et al., Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes, AM J HU GEN, 69(5), 2001, pp. 1033-1045

Authors: Barker, DF

Citation: Df. Barker, Direct genomic multiplex PCR for BRAC1 and application to mutation detection by single-strand conformation and heteroduplex analysis, HUM MUTAT, 16(4), 2000, pp. 334-344

Authors: Bennett, CL Yoshioka, R Kiyosawa, H Barker, DF Fain, PR Shigeoka, AO Chance, PF

Citation: Cl. Bennett et al., X-linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3, AM J HU GEN, 66(2), 2000, pp. 461-468

Authors: Liu, XD Barker, DF

Citation: Xd. Liu et Df. Barker, Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1, AM J HU GEN, 64(5), 1999, pp. 1427-1439