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Results:
1-7
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Results: 7
Authors:
Ruteshouser, EC
Ashworth, LK
Huff, V
Citation: Ec. Ruteshouser et al., Absence of PPP2R1A mutations in Wilms tumor, ONCOGENE, 20(16), 2001, pp. 2050-2054
Authors:
Dharnidharka, VR
Ruteshouser, EC
Rosen, S
Kozakewich, H
Harris, HW
Herrin, JT
Huff, V
Citation: Vr. Dharnidharka et al., Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins, PED NEPHROL, 16(3), 2001, pp. 227-231
Authors:
Green, DM
Breslow, NE
Beckwith, JB
Ritchey, ML
Shamberger, RC
Haase, GM
D'Angio, GJ
Perlman, E
Donaldson, M
Grundy, PE
Weetman, R
Coppes, MJ
Malogolowkin, M
Shearer, P
Coccia, P
Kletzel, M
Thomas, PRM
Macklis, R
Tomlinson, G
Huff, V
Newbury, R
Weeks, D
Citation: Dm. Green et al., Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: A report from the National Wilms' Tumor Study Group, J CL ONCOL, 19(17), 2001, pp. 3719-3724
Authors:
Hussong, JW
Perkins, SL
Huff, V
McDonald, JM
Pysher, TJ
Beckwith, JB
Coffin, CM
Citation: Jw. Hussong et al., Familial Wilms' tumor with neural elements: Characterization by histology,immunohistochemistry, and genetic analysis, PEDIATR D P, 3(6), 2000, pp. 561-567
Authors:
Chao, LY
Huff, V
Strong, LC
Saunders, GF
Citation: Ly. Chao et al., Mutation in the PAX6 gene in twenty patients with aniridia, HUM MUTAT, 15(4), 2000, pp. 332-339
Authors:
Maiti, S
Alam, R
Amos, CI
Huff, V
Citation: S. Maiti et al., Frequent association of beta-catenin and WT1 mutations in Wilms tumors, CANCER RES, 60(22), 2000, pp. 6288-6292
Authors:
El-Naggar, AK
Lai, SL
Tucker, SA
Clayman, GL
Goepfert, H
Hong, WK
Huff, V
Citation: Ak. El-naggar et al., Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma, ONCOGENE, 18(50), 1999, pp. 7063-7069
Risultati:
1-7
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