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Results:
1-11
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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
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