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

Autor RAYNAUD M.
Vydáno C1970

ANNEAUX LOCAUX HENSELIENS.

Autor RAYNAUD M.
Vydáno S1970

ALGEBRAIC GEOMETRY..

Autor RAYNAUD, M
Vydáno S1983

Les fleurs du mal /

Autor Baudelaire, Charles, Raynaud, M. Ernest.
Vydáno 1921.

Les fleurs du mal /

Autor Baudelaire, Charles, Raynaud, M. Ernest.
Vydáno 1958.

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

Autor Relyveld, E. H., Hénocq, E., Raynaud, M.
Vydáno 1964

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

Autor Raynaud, M., Héron, A., Adam, J.-C.
Vydáno v Sci Rep (2020)

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

Autor Matić, D., Skarica, N., Relyveld, E. H., Raynaud, M., Mravunac, B.
Vydáno 1966

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

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

Purification of Bacterial Endotoxins by Zonal Centrifugation

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

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

Autor Babuty, D, Fauchier, L, Tena-Carbi, D, Poret, P, Leche, J, Raynaud, M, Fauchier, J, Cosnay, P
Vydáno 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...

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

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

Autor 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
Vydáno v 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

Autor 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
Vydáno v Mol Psychiatry (2018)

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

Autor 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
Vydáno v Mol Psychiatry (2016)