Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism

Por MANGION, J., EDKINS, S., GOSS, A., STRATTON, M., FLANAGAN, A.
Publicado em 2000

The gene for cherubism maps to chromosome 4p16.3.

Por Mangion, J, Rahman, N, Edkins, S, Barfoot, R, Nguyen, T, Sigurdsson, A, Townend, J V, Fitzpatrick, D R, Flanagan, A M, Stratton, M R
Publicado em 1999

A gene for lymphedema-distichiasis maps to 16q24.3.

Por Mangion, J, Rahman, N, Mansour, S, Brice, G, Rosbotham, J, Child, A H, Murday, V A, Mortimer, P S, Barfoot, R, Sigurdsson, A, Edkins, S, Sarfarazi, M, Burnand, K, Evans, A L, Nunan, T O, Stratton, M R, Jeffery, S
Publicado em 1999

Sparks creating light? Strengthening peripheral disease surveillance in the Democratic Republic of Congo

Por Benedetti, G., Mossoko, M., Nyakio Kakusu, J. P., Nyembo, J., Mangion, J. P., Van Laeken, D., Van den Bergh, R., Van den Boogaard, W., Manzi, M., Kibango, W. K., Hermans, V., Beijnsberger, J., Lambert, V., Kitenge, E.
Publicado no Public Health Action (2016)

Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer.

Por Bignell, G R, Canzian, F, Shayeghi, M, Stark, M, Shugart, Y Y, Biggs, P, Mangion, J, Hamoudi, R, Rosenblatt, J, Buu, P, Sun, S, Stoffer, S S, Goldgar, D E, Romeo, G, Houlston, R S, Narod, S A, Stratton, M R, Foulkes, W D
Publicado em 1997

Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancer

Por SHUGART, Y. Y., COUR, C., RENARD, H., LENOIR, G., GOLDGAR, D., TEARE, D., EASTON, D., RAHMAN, N., GUSTERTON, R., SEAL, S., BARFOOT, R., STRATTON, M., MANGION, J., PEELEN, T., VAN DEN OUWELAND, A., MEIJERS, H., DEVILEE, P., ECCLES, D., LYNCH, H., WEBER, B., STOPPA-LYONNET, D., BIGNON, Y., CHANG-CLAUDE, J.
Publicado em 1999