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Results: 1-10 |
Results: 10

Authors: Guttmacher, AE
Citation: Ae. Guttmacher, Human genetics on the Web, ANN REV GEN, 2, 2001, pp. 213-233

Authors: Jenkins, J Blitzer, M Boehm, K Feetham, S Gettig, E Johnson, A Lapham, EV Patenaude, AF Reynolds, PP Guttmacher, AE
Citation: J. Jenkins et al., Recommendations of core competencies in genetics essential for all health professionals, GENET MED, 3(2), 2001, pp. 155-159

Authors: Rosenberg, MJ Killoran, C Dziadzio, L Chang, S Stone, DL Meck, J Aughton, D Bird, LM Bodurtha, J Cassidy, SB Graham, JM Grix, A Guttmacher, AE Hudgins, L Kozma, C Michaelis, RC Pauli, R Peters, KF Rosenbaum, KN Tifft, CJ Wargowski, D Williams, MS Biesecker, LG
Citation: Mj. Rosenberg et al., Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations, HUM GENET, 109(3), 2001, pp. 311-318

Authors: Guttmacher, AE Jenkins, J Uhlmann, WR
Citation: Ae. Guttmacher et al., Genomic medicine: Who will practice it? A call to open arms, AM J MED G, 106(3), 2001, pp. 216-222

Authors: Collins, FS Guttmacher, AE
Citation: Fs. Collins et Ae. Guttmacher, Genetics moves into the medical mainstream, J AM MED A, 286(18), 2001, pp. 2322-2324

Authors: Guttmacher, AE Collins, FS
Citation: Ae. Guttmacher et Fs. Collins, Genetics resources on the Web (GROW), GENET MED, 2(5), 2000, pp. 296-299

Authors: Guttmacher, AE Callahan, JR
Citation: Ae. Guttmacher et Jr. Callahan, Did Robert Louis Stevenson have hereditary hemorrhagic telangiectasia?, AM J MED G, 91(1), 2000, pp. 62-65

Authors: Shovlin, CL Guttmacher, AE Buscarini, E Faughnan, ME Hyland, RH Westermann, CJJ Kjeldsen, AD Plauchu, H
Citation: Cl. Shovlin et al., Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome), AM J MED G, 91(1), 2000, pp. 66-67

Authors: Guttmacher, AE
Citation: Ae. Guttmacher, Twenty lessons from the heart of medicine, J AM MED A, 284(12), 2000, pp. 1486-1487

Authors: Bourdeau, A Cymerman, U Paquet, ME Meschino, W McKinnon, WC Guttmacher, AE Becker, L Letarte, M
Citation: A. Bourdeau et al., Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1, AM J PATH, 156(3), 2000, pp. 911-923
Risultati: 1-10 |