Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers.

Por Haliassos, A, Chomel, J C, Grandjouan, S, Kruh, J, Kaplan, J C, Kitzis, A
Publicado em 1989

Modification of enzymatically amplified DNA for the detection of point mutations.

Por Haliassos, A, Chomel, J C, Tesson, L, Baudis, M, Kruh, J, Kaplan, J C, Kitzis, A
Publicado em 1989

A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23.

Por Amati, P., Gasparini, P., Zlotogora, J., Zelante, L., Chomel, J. C., Kitzis, A., Kaplan, J., Bonneau, D.
Publicado em 1996

A mesenchymal glioma stem cell profile is related to clinical outcome

Por Balbous, A, Cortes, U, Guilloteau, K, Villalva, C, Flamant, S, Gaillard, A, Milin, S, Wager, M, Sorel, N, Guilhot, J, Bennaceur-Griscelli, A, Turhan, A, Chomel, J-C, Karayan-Tapon, L
Publicado em 2014