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Results:
1-7
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Results: 7
Authors:
Burke, JP
Duggirala, R
Hale, DE
Blangero, J
Stern, MP
Citation: Jp. Burke et al., Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to type 2 diabetes, HUM GENET, 106(5), 2000, pp. 467-472
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:
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:
Lehman, DM
Hale, DE
Cody, JT
Harrison, JM
Leach, RJ
Citation: Dm. Lehman et al., Molecular, morphometric and functional analyses demonstrate that the growth hormone deficient little mouse is not hypomyelinated, DEV BRAIN R, 116(2), 1999, pp. 191-199
Authors:
Trevino, RP
Marshall, RM
Hale, DE
Rodriguez, R
Baker, G
Gomez, J
Citation: Rp. Trevino et al., Diabetes risk factors in low-income Mexican-American children, DIABET CARE, 22(2), 1999, pp. 202-207
Authors:
Burke, JP
Hale, DE
Hazuda, HP
Stern, MP
Citation: Jp. Burke et al., A quantitative scale of acanthosis nigricans, DIABET CARE, 22(10), 1999, pp. 1655-1659
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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