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Results: 4

Authors: Coonen, E Martini, E Dumoulin, JCM Hollanders-Crombach, HTM de Die-Smulders, C Geraedts, JPM Hopman, AHN Evers, JLH
Citation: E. Coonen et al., Preimplantation genetic diagnosis of a reciprocal translocation t(3;11)(q27.3;q24.3) in siblings, MOL HUM REP, 6(3), 2000, pp. 199-206

Authors: Steyaert, J de Die-Smulders, C Fryns, JP Goossens, E Willekens, D Fryns, JP
Citation: J. Steyaert et al., Behavioral phenotype in childhood type of dystrophia myotonica, AM J MED G, 96(6), 2000, pp. 888-889

Authors: Nanni, L Ming, JE Bocian, M Steinhaus, K Bianchi, DW de Die-Smulders, C Giannotti, A Imaizumi, K Jones, KL Del Campo, M Martin, RA Meinecke, P Pierpont, MEM Robin, NH Young, ID Roessler, E Muenke, M
Citation: L. Nanni et al., The mutational spectrum of the Sonic Hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly, HUM MOL GEN, 8(13), 1999, pp. 2479-2488

Authors: Claeys, M Van der Hoeven, M de Die-Smulders, C Bakker, JA Offermans, JPM Forget, PP Groener, JEM Spaapen, LJM
Citation: M. Claeys et al., Early-infantile type of galactosialidosis as a cause of heart failure and neonatal ascites, J INH MET D, 22(5), 1999, pp. 666-667
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