Chorioretinal post-transplant lymphoproliferative disorder induced by the Epstein-Barr virus

Por Demols, P, Cochaux, P, Velu, T, Caspers-Velu, L
Publicado em 2001

DNA fingerprinting in man using a mouse probe related to part of the Drosophila 'Per' gene.

Por Georges, M, Cochaux, P, Lequarre, A S, Young, M W, Vassart, G
Publicado em 1987

A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism.

Por Ieiri, T, Cochaux, P, Targovnik, H M, Suzuki, M, Shimoda, S, Perret, J, Vassart, G
Publicado em 1991

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

Por Obermaier-Kusser, B., Lorenz, B., Schubring, S., Paprotta, A., Zerres, K., Meitinger, T., Meire, F., Cochaux, P., Blankenagel, A., Kommerell, G.
Publicado em 1994

Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.

Por Abramowicz, M J, Targovnik, H M, Varela, V, Cochaux, P, Krawiec, L, Pisarev, M A, Propato, F V, Juvenal, G, Chester, H A, Vassart, G
Publicado em 1992