A new polymorphism in the ret protooncogene (RET)

Por Mulligan, L.M., Gardner, E., Papi, L., Ponder, B.A.J.
Publicado em 1991

Mechanisms of p53 loss in human sarcomas.

Por Mulligan, L M, Matlashewski, G J, Scrable, H J, Cavenee, W K
Publicado em 1990

Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.

Por Sood, R, Mulligan, L M, Poon, R, White, B N, Holden, J J
Publicado em 1990

Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?

Por Fewtrell, M S, Tam, P K, Thomson, A H, Fitchett, M, Currie, J, Huson, S M, Mulligan, L M
Publicado em 1994

Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytoma.

Por Eng, C., Foster, K. A., Healey, C. S., Houghton, C., Gayther, S. A., Mulligan, L. M., Ponder, B. A.
Publicado em 1996

A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h].

Por Wrogemann, K, Arveiler, B, Oberle, I, Mulligan, L M, Holden, J A, Forster-Gibson, C J, White, B N
Publicado em 1986

Mutation and deletion analysis of GFRα-1, encoding the co-receptor for the GDNF/RET complex, in human brain tumours

Por Gimm, O, Gössling, A, Marsh, D J, Dahia, P L M, Mulligan, L M, Deimling, A von, Eng, C
Publicado em 1999

Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.

Por Edery, P, Pelet, A, Mulligan, L M, Abel, L, Attié, T, Dow, E, Bonneau, D, David, A, Flintoff, W, Jan, D
Publicado em 1994

Reduction in membranous immunohistochemical staining for the intracellular domain of epithelial cell adhesion molecule correlates with poor patient outcome in primary colorectal ad...

Por Wang, A., Ramjeesingh, R., Chen, C.H., Hurlbut, D., Hammad, N., Mulligan, L.M., Nicol, C., Feilotter, H.E., Davey, S.
Publicado no Curr Oncol (2016)

Allelic loss on distal chromosome 17p is associated with poor prognosis in a group of Brazilian breast cancer patients.

Por Nagai, M. A., Pacheco, M. M., Brentani, M. M., Marques, L. A., Brentani, R. R., Ponder, B. A., Mulligan, L. M.
Publicado em 1994

Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

Por Mulligan, L M, Phillips, M A, Forster-Gibson, C J, Beckett, J, Partington, M W, Simpson, N E, Holden, J J, White, B N
Publicado em 1985

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

Por Eng, C, Crossey, P A, Mulligan, L M, Healey, C S, Houghton, C, Prowse, A, Chew, S L, Dahia, P L, O'Riordan, J L, Toledo, S P
Publicado em 1995

Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma

Por Feilotter, H E, Coulon, V, McVeigh, J L, Boag, A H, Dorion-Bonnet, F, Duboué, B, Latham1, W C W, Eng, C, Mulligan, L M, Longy, M
Publicado em 1999