Disruption of Neurexin 1 Associated with Autism Spectrum Disorder by Kim, Hyung-Goo, Kishikawa, Shotaro, Higgins, Anne W., Seong, Ihn-Sik, Donovan, Diana J., Shen, Yiping, Lally, Eric, Weiss, Lauren A., Najm, Juliane, Kutsche, Kerstin, Descartes, Maria, Holt, Lynn, Braddock, Stephen, Troxell, Robin, Kaplan, Lee, Volkmar, Fred, Klin, Ami, Tsatsanis, Katherine, Harris, David J., Noens, Ilse, Pauls, David L., Daly, Mark J., MacDonald, Marcy E., Morton, Cynthia C., Quade, Bradley J., Gusella, James F.

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Undiagnosed Phenylketonuria Can Exist Everywhere: Results From an International Survey by van Wegberg, Annemiek M.J., Trefz, Friedrich, Gizewska, Maria, Ahmed, Sibtain, Chabraoui, Layachi, van Spronsen, Francjan J., Al Mutairi, F., Arnoux, J.B., Ballhausen, D., Baruteau, J., Bernstein, L., Bijarnia-Mahay, S., Bordugo, A., Brodosi, L., Brooks, S., Chew, H.B., Chyz, K., Coker, M., Collingwood, C., Cornejo, V., Cozens, A., Das, A.M., de las Heras Montero, J., Debray, F.G., Dercksen, M., Descartes, M., Eminoglu, F.T., Enns, G.M., Ford, S., Freisinger, P., Grafakou, O., Gramer, G., Gray, S., Groselj, U., Grünert, S.C., Haas, D., Handoom, B., Harte, T.B., Hendriksz, C., Hoi-Yee Wu, T., Jamuar, S.S., Jonsson, J.J., Jovanovic, A., Kern, I., Kilavuz, S., Knerr, I., Korycinska-Chaaban, D., Kreile, M., Kumru, B., Lanpher, B., Lapatto, R., Leao-Teles, E., Leuzzi, V., Longo, N., Lopez-Uriarte, A., Lubout, C.M.A., MacDonald, A., Mitchell, J., Mochel, F., Morris, A., Moura de Souza, C.F., Munoz, T., Oscarson, M., Õunap, K., Paci, S., Pastores, G.M., Pearl, P.L., Pitt, J., Poon, G., Presner, N., Rabaty, A.A., Reinson, K., Reismann, P., Rink, T., Rocha, J.C., Rodrigues, E., Saini, A.G., Sander, J., Schwartz, I.V.D., Sharma, R., Siriwardena, K., Sirrs, S., Sjarif, D.R., Sondheimer, N., Sparkes, R., Specola, N., Stepien, K.M., Szatmari, I., Tchan, M., Valle, M.G., Vela-Amieva, M., Verdaguer, M.L., Vergano, S.A., Vermeersch, P., Wagenmakers, M.A.E.M., Weinhold, N., Wilson, W.G., Zafeiriou, D., Zhang, H., Ziagaki, A.

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La protéomique, une nouvelle technique pour un typage optimal des amyloses by Colombat, M., Holifanjaniaina, S., Onifarasoaniaina, S., Valleix, S., Maisonneuve, H., Kahn, J.E.

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Œuvres de Descartes

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Méditations métaphysiques touchant l'opération de Dieu dans l'ordre de la nature, où l'on explique d'une manière claire et méthodique les plus importantes vérités de la métaphysiqu...

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The fronto-ocular syndrome: second mother-daughter case by Descartes, M, Franklin, J

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Uvéite au cours d'un traitement par acide zolédronique : une observation by Banal, F., Briot, K., Bourhis, A., Ayoub, G., Chehensse, C., Escalas, C., Trijau, S., Grangeon, E., Dougados, M., Roux, C.

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Identification of a recombination event narrowing the Lafora disease gene region by Maddox, L O, Descartes, M, Collins, J, Keating, J, Rosenfeld, S, Palmer, C, Carroll, A J, Kuzniecky, R

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Discours de la methode pour bien conduire sa raison, & chercher la verité dans les sciences. Plus La dioptriqve. Les meteores. Et La geometrie. Qui sont des essais de cete methode

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AsktheGeneticistSM: five years of online experience by Tesla, Catherine, Korf, Bruce R., Holt, Lynn, Prucka, Sandra, Robin, Nathaniel H., Descartes, Maria, Lose, Edward, Stembridge, Adrya, Epstein, Michael, Warren, Stephen

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Traité de la mechanique

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Congenital diaphragmatic hernia: Is 15q26.1-26.2 a candidate locus? by Biggio Jr, Joseph R., Descartes, Maria D., Carroll, Andrew J., Holt, R. Lynn

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Monosomy1p36.3 and Trisomy 19p13.3 in a Child With Periventricular Nodular Heterotopia by Descartes, Maria, MD, Mikhail, Fady M., MD, PhD, Franklin, Judith C., MSN, McGrath, Tony M., MD, Bebin, Martina, MD, MPA

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Mosaicism for duplication of 17q21 · qter with lymphedema and normal phenotype by Descartes, M., Baldwin, L., Cosper, P., Carroll, A.

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A five-year experience with fragile X screening of high-risk gravid women by Wenstrom, Katharine D., Descartes, Maria, Franklin, Judy, Cliver, Suzanne P.

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Comparison of SSCP analysis and CFLP analysis for mutation detection in the human iduronate 2-sulfatase gene by Maddox, L O, Li, P, Bennett, A, Descartes, M, Thompson, J N

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Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles by Brown, T. C., Tarleton, J. C., Go, R. C. P., Longshore, J. W., Descartes, M.

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The fronto-ocular syndrome: second mother-daughter case by Descartes, M, Franklin, J

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Plants of New Caledonia. CXXI. Iridoids and alkaloids of Plectronia odorata. [French by Gournelis D, Skaltsounis A.L, Tillequin F, Koch M, Pusset J, Labarre S

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Strategies to increase the donor pool and access to kidney transplantation: an international perspective by Maggiore, Umberto, Oberbauer, Rainer, Pascual, Julio, Viklicky, Ondrej, Dudley, Chris, Budde, Klemens, Sorensen, Soren Schwartz, Hazzan, Marc, Klinger, Marian, Abramowicz, Daniel

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