Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation.

Por Rousseau, F, Heitz, D, Oberlé, I, Mandel, J L
Publicado em 1991

Rapid PCR analysis of the St14 (DXS52) VNTR.

Por Richards, B, Heilig, R, Oberlé, I, Storjohann, L, Horn, G T
Publicado em 1991

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.

Por Oberlé, I, Drayna, D, Camerino, G, White, R, Mandel, J L
Publicado em 1985

Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.

Por Feil, R, Palmieri, G, d'Urso, M, Heilig, R, Oberlé, I, Mandel, J L
Publicado em 1990

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.

Por Arveiler, B, Oberlé, I, Vincent, A, Hofker, M H, Pearson, P L, Mandel, J L
Publicado em 1988

Localization of the mcf.2 transforming sequence to the X chromosome.

Por Noguchi, T, Mattei, M G, Oberlè, I, Planche, J, Imbert, J, Pelassy, C, Birg, F, Birnbaum, D
Publicado em 1987

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

Molecular cloning and analysis of the fragile X region in man.

Por Dietrich, A, Kioschis, P, Monaco, A P, Gross, B, Korn, B, Williams, S V, Sheer, D, Heitz, D, Oberle, I, Toniolo, D
Publicado em 1991

Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.

Por de Saint Basile, G, Arveiler, B, Oberlé, I, Malcolm, S, Levinsky, R J, Lau, Y L, Hofker, M, Debre, M, Fischer, A, Griscelli, C
Publicado em 1987

Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)

Por Rousseau, F., Vincent, A., Rivella, S., Heitz, D., Triboli, C., Maestrini, E., Warren, S. T., Suthers, G. K., Goodfellow, P., Mandel, J. L., Toniolo, D., Oberle, I.
Publicado em 1991

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.

Por Oberlé, I, Heilig, R, Moisan, J P, Kloepfer, C, Mattéi, G M, Mattéi, J F, Boué, J, Froster-Iskenius, U, Jacobs, P A, Lathrop, G M
Publicado em 1986

Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines

Por Suthers, G. K., Hyland, V. J., Callen, D. F., Oberle, I., Rocchi, M., Thomas, N. S., Morris, C. P., Schwartz, C. E., Schmidt, M., Ropers, H. H., Baker, E., Oostra, B. A., Dahl, N., Wilson, P. J., Hopwood, J. J., Sutherland, G. R.
Publicado em 1990