Results: 1-11 |
Results: 11

Authors: Pagon, RA Pinsky, L Beahler, CC
Citation: Ra. Pagon et al., Online medical genetics resources: a US perspective, BR MED J, 322(7293), 2001, pp. 1035-1037

Authors: Hanna, JAS Ball, S Pagon, RA Donlan, M
Citation: Jas. Hanna et al., Mother to son transmission of del(1) (q42.1q42.3), AM J MED G, 98(1), 2001, pp. 103-106

Authors: Pagon, RA Hanson, NB Neufeld-Kaiser, W Covington, ML
Citation: Ra. Pagon et al., Genetic consultation, WEST J MED, 174(6), 2001, pp. 397-399

Authors: Pagon, RA Pinsky, L
Citation: Ra. Pagon et L. Pinsky, The helix and health: applying genetics to primary care, WEST J MED, 174(5), 2001, pp. 304-304

Authors: Pagon, RA Hanson, NB Neufeld-Kaiser, W Covington, ML
Citation: Ra. Pagon et al., Genetic testing, WEST J MED, 174(5), 2001, pp. 344-347

Authors: Tarczy-Hornoch, P Shannon, P Baskin, P Espeseth, M Pagon, RA
Citation: P. Tarczy-hornoch et al., GeneClinics: A hybrid text/data electronic publishing model using XML applied to clinical genetic testing, J AM MED IN, 7(3), 2000, pp. 267-276

Authors: Belleh, S Zhou, GM Wang, M Der Kaloustian, VM Pagon, RA Godfrey, M
Citation: S. Belleh et al., Two novel fibrillin-2 mutations in congenital contractural arachnodactyly, AM J MED G, 92(1), 2000, pp. 7-12

Authors: Pagon, RA Tarczy-Hornoch, P
Citation: Ra. Pagon et P. Tarczy-hornoch, The virtues of the virtual world, GENET MED, 1(5), 1999, pp. 177-177

Authors: Smith, W Ji, HLP Mouradian, W Pagon, RA
Citation: W. Smith et al., Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL): Presentation in two unrelated patients in the United States, AM J MED G, 86(3), 1999, pp. 245-252

Authors: Dinulos, MB Pagon, RA
Citation: Mb. Dinulos et Ra. Pagon, Autosomal dominant inheritance of Barber-Say syndrome, AM J MED G, 86(1), 1999, pp. 54-56

Authors: Kawame, H Hannibal, MC Hudgins, L Pagon, RA
Citation: H. Kawame et al., Phenotypic spectrum and management issues in Kabuki syndrome, J PEDIAT, 134(4), 1999, pp. 480-485
Risultati: 1-11 |