Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation. Borck, G., Rio, M., Sanlaville, D., Redon, R., Molinari, F., Bacq, D., Raoul, O., Cormier-Daire, V., Lyonnet, S., Amiel, J., Merrer, M. L., Blois, M. C. d., Prieur, M., Vekemans, M., Carter, N. P., Munnich, A., & Colleaux, L. Clin. Genet., 66(2):122-127, 2004. bibtex @Article{Borck_2004_6760,
author = {Borck, G. and Rio, M. and Sanlaville, D. and Redon, R. and Molinari, F. and Bacq, D. and Raoul, O. and Cormier-Daire, V. and Lyonnet, S. and Amiel, J. and Merrer, M. Le and Blois, M. C. de and Prieur, M. and Vekemans, M. and Carter, N. P. and Munnich, A. and Colleaux, L.},
journal = {Clin. Genet.},
number = {2},
pages = {122-127},
title = {Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation},
volume = {66},
year = {2004},
title_with_no_special_chars = {Genomewide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation}
}
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