Authors:
Schmitt, W
Baissa, E
Mandel, A
Anson, CE
Powell, AK
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Authors:
Osborne, LR
Li, M
Pober, B
Chitayat, D
Bodurtha, J
Mandel, A
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Scherer, SW
Citation: Lr. Osborne et al., A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome, NAT GENET, 29(3), 2001, pp. 321-325
Authors:
Tentler, D
Gustavsson, P
Elinder, G
Eklof, O
Gordon, L
Mandel, A
Dahl, N
Citation: D. Tentler et al., A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome, J MED GENET, 37(2), 2000, pp. 128-131
Citation: T. Labahn et al., On the insertion into the lanthanide-carbon bond. Synthesis and structure of [(Cp2Sm)-Sm-(C6H5CH2NNO)](2) and [K(18-crown-6)(Cp2Yb)-Yb-* (NCS)(2)](infinity), Z ANORG A C, 625(8), 1999, pp. 1273-1277
Authors:
Mandel, A
Schmitt, W
Womack, TG
Bhalla, R
Henderson, RK
Heath, SL
Powell, AK
Citation: A. Mandel et al., A bioinspired approach to control over size, shape and function of polynuclear iron compounds, COORD CH RE, 192, 1999, pp. 1067-1083