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Results: 4

Authors: Bolk, S Pelet, A Hofstra, RMW Angrist, M Salomon, R Croaker, D Buys, CHCM Lyonnet, S Chakravarti, A
Citation: S. Bolk et al., A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus, P NAS US, 97(1), 2000, pp. 268-273

Authors: Southard-Smith, EM Angrist, M Ellison, JS Agarwala, R Baxevanis, AD Chakravarti, A Pavan, WJ
Citation: Em. Southard-smith et al., The Sox10(Dom) mouse: Modeling the genetic variation of Waardenburg-Shah (WS4) syndrome, GENOME RES, 9(3), 1999, pp. 215-225

Authors: Angrist, M Bolk, S Bentley, K Nallasamy, S Halushka, MK Chakravarti, A
Citation: M. Angrist et al., Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease, ONCOGENE, 17(23), 1998, pp. 3065-3070

Authors: Chadwick, BP Helbling, LA Angrist, M Chakravarti, A Gusella, JF Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR, CYTOG C GEN, 83(3-4), 1998, pp. 236-237
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