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Publications of 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.

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