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

gan RAYNAUD M.
Cyhoeddwyd C1970

ANNEAUX LOCAUX HENSELIENS.

gan RAYNAUD M.
Cyhoeddwyd S1970

ALGEBRAIC GEOMETRY..

gan RAYNAUD, M
Cyhoeddwyd S1983

Les fleurs du mal /

gan Baudelaire, Charles, Raynaud, M. Ernest.
Cyhoeddwyd 1921.

Les fleurs du mal /

gan Baudelaire, Charles, Raynaud, M. Ernest.
Cyhoeddwyd 1958.

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

gan Relyveld, E. H., Hénocq, E., Raynaud, M.
Cyhoeddwyd 1964

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

gan Raynaud, M., Héron, A., Adam, J.-C.
Cyhoeddwyd yn Sci Rep (2020)

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

gan Matić, D., Skarica, N., Relyveld, E. H., Raynaud, M., Mravunac, B.
Cyhoeddwyd 1966

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

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

Purification of Bacterial Endotoxins by Zonal Centrifugation

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

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

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

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

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

gan 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
Cyhoeddwyd yn 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

gan 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
Cyhoeddwyd yn Mol Psychiatry (2018)

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

gan 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
Cyhoeddwyd yn Mol Psychiatry (2016)