Publicaciones 1998

Bernot A., Da Silva C., Petit J.L., Cruaud C., Caloustian C., Castet V., Ahmed-Arab M., Dross C., Dupont M., Cattan D., Smaoui N., Dode C., Pecheux C., Nedelec B., Medaxian J., Rozenbaum M., Rosner I., Delpech M., Grateau G., Demaille J., Weissenbach J. and Touitou I.
 «Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF)»
 Hum. Mol. Genet. 1998. 7:1317-25.

Bernot A., Heilig R., Clepet C., Smaoui N., Da Silva C., Petit J.L., Devaud C., Chiannilkulchai N., Fizames C., Samson D., Cruaud C., Caloustian C., Gyapay G., Delpech M. and Weissenbach J.
 «A transcriptional Map of the FMF region»
 Genomics. 1998. 50:147-60.

Deloukas P., Schuler G.D., Gyapay G., Beasley E.M., Soderlund C., Rodriguez-Tomé P., Hui L., Matise T.C., McKusick K.B., Bentolila S., Bihoreau M.T., Birren B.B., Browne J., Butler A., Castle A.B., Chiannilkulchai N., Clee C., Day P.J.R., Dehejia A., Bibling T., Drouot N., Duprat S., Fizames C., Fox S., Gelling S., Green L., Harrison P., Hocking R., Holloway E., Hunt S., Keil S., Lijnzaad P., Louis-Dit-Sully C., Ma J., Mendis A., Miller J., Morissette J., Muselet D., Nusbaum H.C., Peck A., Rozen S., Simon D., Slonim D.K., Staples R., Stein L.D., Stewart E.A., Suchard M.A., Thangarajah T., Vega-Czarny N., Webber C., Wu X., Hudson J., Auffray C., Nomura N., Sikela J.M., Polymeropoulos M.H., James M.R., Lander E.S., Hudson T.J., Myers R.M., Cox D.R., Weissenbach J., Boguski M.S. and Bentley D.R.
 «A physical map of 30,000 human genes»
 Science. 1998. 282:744-746.

Dewalle M., Domingo C., Rozenbaum M., Ben-Chétrit E., Cattan D., Bernot A., Dross C., Dupont M., Notarnicola C., Levy M., Rosner I., Demaille J. and Touitou I.
 «Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF)»
 Eur. J. Human Genet. 1998. 6:95-97.

Fischer J., Bouadjar B., Heilig R., Fizames C., Prud’homme J.F. and Weissenbach J.
 «Genetic linkage of Meleda disease to chromosome 8qter»
 Eur. J. Human Genet. 1998. 6:542-547.

Fischer J., Urtizberea J.A., Pavek S., Vandiedonck C., Brüls T., Saker S., Alkatip Y., Prud’homme J.F. and Weissenbach J.
 «Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22»
 Hum. Genet. 1998. 103:60-64.

Mustapha M., Chardenoux S., Nieder A., Salem N., Weissenbach J., El-Zir E., Loiselet J. and Petit C.
 «A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36»
 Eur. J. Human Genet. 1998. 6:245-250.

Paternotte C., Rudnicki D., Fizames C., Davoine C.S., Mavel D., Durr A., Samson D., Marquette C., Muselet D., Vega-Czarny N., Drouot N., Voit T., Fontaine B., Gyapay G., Auburger G., Weissenbach J. and Hazan J.
 «Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q»
 Genome Res. 19998. 8:1216-1227.

Pawlak A., Chiannikulchai N., Ansorge W., Bulle F., Weissenbach J., Gyapay G. and Guellaën G.
 «Identification and mapping of 26 human testis mRNAs containing CAG/CTG repeats»
 Mamm. Genome. 1998. 9:745-8.

Salomon-Nguyen F., Le Coniat-Busson M., Heilig R., Campion D., Weissenbach J. and Berger R.
 «Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNA»
 C. R. Acad. Sci. III. 1998. 321:447-52 (1998).

Weissenbach J.
 «Human genome mapping and sequencing: perspectives for toxicology»
 Toxicol. Lett. 1998. 102-103:1-4 (1998).

Weissenbach J.
 «The Human Genome Project: from mapping to sequencing»
 Clin. Chem. Lab. Med. 1998. 36:511-4.