Хайлтын үр дүнгүүд - Van Dop, C
- 8-н 1 - 8 үр дүнгүүдийг харуулж байна
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Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy. -н Levine, M A, Ahn, T G, Klupt, S F, Kaufman, K D, Smallwood, P M, Bourne, H R, Sullivan, K A, Van Dop, C
Хэвлэсэн 1988текст -
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An arginine to histidine mutation in codon 311 of the C-erbA beta gene results in a mutant thyroid hormone receptor that does not mediate a dominant negative phenotype. -н Geffner, M E, Su, F, Ross, N S, Hershman, J M, Van Dop, C, Menke, J B, Hao, E, Stanzak, R K, Eaton, T, Samuels, H H
Хэвлэсэн 1993текст