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Results:
1-7
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Results: 7
Authors:
Lehman, DM
Sponsel, WE
Stratton, RF
Mensah, J
Macdonald, JC
Johnson-Pais, TL
Coon, H
Reveles, XT
Cody, JD
Leach, RJ
Citation: Dm. Lehman et al., Genetic mapping of a novel X-linked recessive colobomatous microphthalmia, AM J MED G, 101(2), 2001, pp. 114-119
Authors:
Hale, DE
Cody, JD
Baillargeon, J
Schaub, R
Danney, MM
Leach, RJ
Citation: De. Hale et al., The spectrum of growth abnormalities 18q deletions, J CLIN END, 85(12), 2000, pp. 4450-4454
Authors:
Leach, RJ
Singer, FR
Cody, JD
Roodman, GD
Citation: Rj. Leach et al., Variable disease severity associated with a Paget's disease predispositiongene, J BONE MIN, 14, 1999, pp. 17-20
Authors:
Cody, JD
Reveles, XT
Hale, DE
Lehman, D
Coon, H
Leach, RJ
Citation: Jd. Cody et al., Haplosufficiency of the melanocortin-4 receptor gene in individuals with deletions of 18q, HUM GENET, 105(5), 1999, pp. 424-427
Authors:
Wang, ZQ
Cody, JD
Leach, RJ
O'Connell, P
Citation: Zq. Wang et al., Gene expression patterns in cell lines from patients with 18q-syndrome, HUM GENET, 104(6), 1999, pp. 467-475
Authors:
Cody, JD
Hutcheon, IE
Krouse, HR
Citation: Jd. Cody et al., Fluid flow, mixing and the origin of CO2 and H2S by bacterial sulphate reduction in the Mannville Group, southern Alberta, Canada, MAR PETR G, 16(6), 1999, pp. 495-510
Authors:
Cody, JD
Ghidoni, PD
DuPont, BR
Hale, DE
Hilsenbeck, SG
Stratton, RF
Hoffman, DS
Muller, S
Schaub, RL
Leach, RJ
Kaye, CI
Citation: Jd. Cody et al., Congenital anomalies and anthropometry of 42 individuals with deletions ofchromosome 18q, AM J MED G, 85(5), 1999, pp. 455-462
Risultati:
1-7
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