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Results: 1-3 |
Results: 3
Novel point mutation (W184R) in neonatal type 2 Gaucher disease
Authors: Choy, FYM Wong, K Vallance, HD Baldwin, V
Citation: Fym. Choy et al., Novel point mutation (W184R) in neonatal type 2 Gaucher disease, PEDIATR D P, 3(2), 2000, pp. 180-183
Year 2000 engineering in BT
Authors: Wiggins, A Green, T Baldwin, V
Citation: A. Wiggins et al., Year 2000 engineering in BT, BR TEL ENG, 18, 1999, pp. 52-58
Frequency of the codon 807 mutation in the cGMP phosphodiesterase beta-subunit gene in Irish setters and other dog breeds with hereditary retinal degeneration
Authors: Aguirre, GD Baldwin, V Weeks, KM Acland, GM Ray, K
Citation: Gd. Aguirre et al., Frequency of the codon 807 mutation in the cGMP phosphodiesterase beta-subunit gene in Irish setters and other dog breeds with hereditary retinal degeneration, J HEREDITY, 90(1), 1999, pp. 143-147
Risultati: 1-3 |