| |
| | Ethylin Wang Jabs' Lab: Publications |
 | | Tavormina, P., Bellus, G.A., Webster, MK., Bamshad, M.J., Fraley, A.E., McIntosh, I., Szabo, J., Jiang, W., Jabs, E.W., Wilcox, W.R., Wasmuth, J.J., Donoghue, D.J., Thompson, L.M.,and Francomanco, C.A. A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in fibroblast growth factor receptor 3 gene. |
 | | Howard, T.D., Guttmacher, A.E., McKinnon, W., Sharma, M., McKusick, V.A., and Jabs, E.W. Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus. |
 | | Craig, R.W., Jabs, E.W., Zhou, P., Kozopas, K.M., Hawkins, A.L., Rochelle, J.M., Seldin, M.F., and Griffin, C.A. Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MCL1 maps to human chromosome 1q21, a region that is frequently altered in preneoplastic and neoplastic disease. |
| www.hopkinsmedicine.org /JabsLab/Publications.cfm (4905 words) |
|