Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.

Por Richards, R I, Holman, K, Kozman, H, Kremer, E, Lynch, M, Pritchard, M, Yu, S, Mulley, J, Sutherland, G R
Publicado em 1991

Prevention of bleomycin-induced pulmonary fibrosis after adenovirus-mediated transfer of the bacterial bleomycin resistance gene.

Por Tran, P L, Weinbach, J, Opolon, P, Linares-Cruz, G, Reynes, J P, Grégoire, A, Kremer, E, Durand, H, Perricaudet, M
Publicado em 1997

Fragile-X syndrome: Unique genetics of the heritable unstable element

Por Yu, S., Mulley, J., Loesch, D., Turner, G., Donnelly, A., Gedeon, A., Hillen, D., Kremer, E., Lynch, M., Pritchard, M., Sutherland, G. R., Richards, R. I.
Publicado em 1992

Isolation of a human DNA sequence which spans the fragile X

Por Kremer, E. J., Yu, S., Pritchard, M., Nagaraja, R., Heitz, D., Lynch, M., Baker, E., Hyland, V. J., Little, R. D., Wada, M., Toniolo, D., Vincent, A., Rousseau, F., Schlessinger, D., Sutherland, G. R., Richards, R. I.
Publicado em 1991