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