FAISCEAUX AMPLES SUR LES SCHEMAS EN GROUPES ET LES ESPACES HOMOGENES.

by RAYNAUD M.
Published C1970

ANNEAUX LOCAUX HENSELIENS.

by RAYNAUD M.
Published S1970

ALGEBRAIC GEOMETRY..

by RAYNAUD, M
Published S1983

Les fleurs du mal /

by Baudelaire, Charles, Raynaud, M. Ernest.
Published 1921.

Les fleurs du mal /

by Baudelaire, Charles, Raynaud, M. Ernest.
Published 1958.

Etude de la vaccination antidiphtérique de sujets allergiques, avec une anatoxine pure adsorbée sur phosphate de calcium

by Relyveld, E. H., Hénocq, E., Raynaud, M.
Published 1964

Excitation of surface plasma waves and fast electron generation in relativistic laser–plasma interaction

by Raynaud, M., Héron, A., Adam, J.-C.
Published in Sci Rep (2020)

Etude du pouvoir vaccinant de l'anatoxine diphtérique purifiée sur des adjuvants divers.

by Matić, D., Skarica, N., Relyveld, E. H., Raynaud, M., Mravunac, B.
Published 1966

GROUPES DE MONODROMIE EN GEOMETRIE ALGEBRIQUE (SGA7,1).

by Séminaire de Geometrie Algebraique du Bois Marie, Raynaud, M., Grothendieck, A., Rim, D. S.
Published 1972.

Purification of Bacterial Endotoxins by Zonal Centrifugation

by Mendiola, L. R., Kouznetzova, B., Chermann, J.-C., Sinoussi, F., Digeon, M., Raynaud, M.
Published 1972

Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods?

by Babuty, D, Fauchier, L, Tena-Carbi, D, Poret, P, Leche, J, Raynaud, M, Fauchier, J, Cosnay, P
Published 1999

A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded pat...

by Longo, I, Frints, S, Fryns, J, Meloni, I, Pescucci, C, Ariani, F, Borghgraef, M, Raynaud, M, Marynen, P, Schwartz, C, Renieri, A, Froyen, G
Published 2003

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

by Nguyen, LS, Jolly, L, Shoubridge, C, Chan, WK, Huang, L, Laumonnier, F, Raynaud, M, Hackett, A, Field, M, Rodriguez, J, Srivastava, AK, Lee, Y, Long, R, Addington, AM, Rapoport, JL, Suren, S, Hahn, CN, Gamble, J, Wilkinson, MF, Corbett, MA, Gecz, J
Published in Mol Psychiatry (2011)

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

by Palmer, E E, Stuhlmann, T, Weinert, S, Haan, E, Van Esch, H, Holvoet, M, Boyle, J, Leffler, M, Raynaud, M, Moraine, C, van Bokhoven, H, Kleefstra, T, Kahrizi, K, Najmabadi, H, Ropers, H-H, Delgado, M R, Sirsi, D, Golla, S, Sommer, A, Pietryga, M P, Chung, W K, Wynn, J, Rohena, L, Bernardo, E, Hamlin, D, Faux, B M, Grange, D K, Manwaring, L, Tolmie, J, Joss, S, Cobben, J M, Duijkers, F A M, Goehringer, J M, Challman, T D, Hennig, F, Fischer, U, Grimme, A, Suckow, V, Musante, L, Nicholl, J, Shaw, M, Lodh, S P, Niu, Z, Rosenfeld, J A, Stankiewicz, P, Jentsch, T J, Gecz, J, Field, M, Kalscheuer, V M
Published in Mol Psychiatry (2018)

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

by Hu, H, Haas, S A, Chelly, J, Van Esch, H, Raynaud, M, de Brouwer, A P M, Weinert, S, Froyen, G, Frints, S G M, Laumonnier, F, Zemojtel, T, Love, M I, Richard, H, Emde, A-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, M A, Gardner, A, Willis-Owen, S, Tan, C, Friend, K L, Belet, S, van Roozendaal, K E P, Jimenez-Pocquet, M, Moizard, M-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, van Bömmel, A, Göke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Müller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bieleńska, A, Ousager, L B, Wieacker, P, Rodríguez Criado, G, Bondeson, M-L, Annerén, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, J-P, Devriendt, K, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, T F, Tzschach, A, van Bokhoven, H, Gecz, J, Jentsch, T J, Chen, W, Ropers, H-H, Kalscheuer, V M
Published in Mol Psychiatry (2016)