David Ng
Division of Cancer Epidemiology and Genetics
National Cancer Institute
NIH, DHHS, Bethesda
Maryland
USA
Name/email consistency: high
- Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes. Ng, D., Yang, X.R., Tucker, M.A., Goldstein, A.M. BMC. Res. Notes (2008)
- Replication of a genome-wide case-control study of esophageal squamous cell carcinoma. Ng, D., Hu, N., Hu, Y., Wang, C., Giffen, C., Tang, Z.Z., Han, X.Y., Yang, H.H., Lee, M.P., Goldstein, A.M., Taylor, P.R. Int. J. Cancer (2008)
- High-density mapping and follow-up studies on chromosomal regions 1, 3, 6, 12, 13 and 17 in 28 families with chronic lymphocytic leukaemia. Ng, D., Marti, G.E., Fontaine, L., Toro, J.R., Caporaso, N., Goldin, L.R. Br. J. Haematol. (2006)
- Retrospective family study of childhood medulloblastoma. Ng, D., Stavrou, T., Liu, L., Taylor, M.D., Gold, B., Dean, M., Kelley, M.J., Dubovsky, E.C., Vezina, G., Nicholson, H.S., Byrne, J., Rutka, J.T., Hogg, D., Reaman, G.H., Goldstein, A.M. Am. J. Med. Genet. A (2005)