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:
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:
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