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Results: 1-11 |
Results: 11
The hedgehog pathway and basal cell carcinomas
Authors: Bale, AE Yu, KP
Citation: Ae. Bale et Kp. Yu, The hedgehog pathway and basal cell carcinomas, HUM MOL GEN, 10(7), 2001, pp. 757-762
Treatment of a thyrotropinoma with octreotide-LAR in a patient with multiple endocrine neoplasia-1
Authors: Taylor, TJ Donlon, SS Bale, AE Smallridge, RC Francis, TB Christensen, RS Burman, KD
Citation: Tj. Taylor et al., Treatment of a thyrotropinoma with octreotide-LAR in a patient with multiple endocrine neoplasia-1, THYROID, 10(11), 2000, pp. 1001-1007
Modeling aquatic mercury fate in Clear Lake, Calif.
Authors: Bale, AE
Citation: Ae. Bale, Modeling aquatic mercury fate in Clear Lake, Calif., J ENV ENG, 126(2), 2000, pp. 153-163
Cancer - Sheep, lilies and human genetics
Authors: Bale, AE
Citation: Ae. Bale, Cancer - Sheep, lilies and human genetics, NATURE, 406(6799), 2000, pp. 944-945
PTCH gene mutations in odontogenic keratocysts
Authors: Barreto, DC Gomez, RS Bale, AE Boson, WL De Marco, L
Citation: Dc. Barreto et al., PTCH gene mutations in odontogenic keratocysts, J DENT RES, 79(6), 2000, pp. 1418-1422
Direct molecular diagnosis of multiple endocrine neoplasia type 1
Authors: Petty, EM Glynn, M Bale, AE
Citation: Em. Petty et al., Direct molecular diagnosis of multiple endocrine neoplasia type 1, METH MOL M, 49, 2000, pp. 227-242
Medium-chain acyl-CoA dehydrogenase deficiency: Sudden and unexpected death of a 45 year old woman
Authors: Raymond, K Bale, AE Barnes, CA Rinaldo, P
Citation: K. Raymond et al., Medium-chain acyl-CoA dehydrogenase deficiency: Sudden and unexpected death of a 45 year old woman, GENET MED, 1(6), 1999, pp. 293-294
Prenatal diagnosis of ornithine transcarbamylase deficiency
Authors: Bale, AE
Citation: Ae. Bale, Prenatal diagnosis of ornithine transcarbamylase deficiency, PRENAT DIAG, 19(11), 1999, pp. 1052-1054
Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G
Authors: Topaloglu, AK Sansaricq, C Fox, JE Bale, AE Tuchman, M Desnick, RJ
Citation: Ak. Topaloglu et al., Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G, J INH MET D, 22(1), 1999, pp. 82-83
Mutational analyses of candidate genes in human squamous cell carcinomas
Authors: Petroianu, A Boson, WL Bale, AE Friedman, E De Marco, L
Citation: A. Petroianu et al., Mutational analyses of candidate genes in human squamous cell carcinomas, LARYNGOSCOP, 109(4), 1999, pp. 661-663
Familial medullary thyroid carcinoma: Presymptomatic diagnosis and management in children
Authors: Heptulla, RA Schwartz, RP Bale, AE Flynn, D Genel, M
Citation: Ra. Heptulla et al., Familial medullary thyroid carcinoma: Presymptomatic diagnosis and management in children, J PEDIAT, 135(3), 1999, pp. 327-331
Risultati: 1-11 |