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Results: 1-5 |
Results: 5

Authors: Kates, WR Burnette, CP Jabs, EW Rutberg, J Murphy, AM Grados, M Geraghty, M Kaufmann, WE Pearlson, GD
Citation: Wr. Kates et al., Regional cortical white matter reductions in velocardiofacial syndrome: A volumetric MRI analysis, BIOL PSYCHI, 49(8), 2001, pp. 677-684

Authors: Cargile, CB McIntosh, I Clough, MV Rutberg, J Yaghmai, R Goodman, BK Chen, XN Korenberg, JR Thomas, GH Geraghty, MT
Citation: Cb. Cargile et al., Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12), AM J MED G, 92(5), 2000, pp. 328-335

Authors: Goodman, BK Rutberg, J Lin, WW Pulver, AE Thomas, GH Geraghty, MT
Citation: Bk. Goodman et al., Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome, J INH MET D, 23(8), 2000, pp. 847-848

Authors: Sigurdardottir, S Goodman, BK Rutberg, J Thomas, GH Jabs, EW Geraghty, MT
Citation: S. Sigurdardottir et al., Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of ''complete ring" syndrome, AM J MED G, 87(5), 1999, pp. 384-390

Authors: Goodman, BK Shaffer, LG Rutberg, J Leppert, M Harum, K Gagos, S Ray, JH Bialer, MG Zhou, XT Pletcher, BA Shapira, SK Geraghty, MT
Citation: Bk. Goodman et al., Inherited duplication Xq27-qter at Xp22.3 in severely affected males: Molecular cytogenetic evaluation and clinical description in three unrelated families, AM J MED G, 80(4), 1998, pp. 377-384
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