Browse by Author Mandel, A
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| Title | Author(s) | Year | View Count |  | Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patients | Wu, YQ; Bejjani, BA; Tsui, LC; Mandel, A; Osborne, LR; Shaffer, LG | 2002 | 206 |
| A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome | Osborne, LR; Li, M; Pober, B; Chitayat, D; Bodurtha, J; Mandel, A; Costa, T; Grebe, T; Cox, S; Tsui, LC; Scherer, SW | 2001 | 1,758 |
| Influence of restraint stress on the expression and the serine/threonine phosphatase activity of calcineurin in the rat brain | Wu, YQ; Bejjani, BA; Tsui, LC; Mandel, A; Osborne, LR; Shaffer, LG | 2001 | 41 |
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