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21.
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- Kieffer, V
- Bienvenu, T
- Vinet, M C
- Beldjord, C
- Kahn, A
- Ponsot, G
- Chelly, J
- Moutard, M L
Producer: 19980709
In:
Clinical genetics vol. 53
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22.
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MECP2 mutations account for most cases of typical forms of Rett syndrome. [electronic resource] by
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- Vinet, M C
- Jonveaux, P
- Couvert, P
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- Beldjord, C
- Fontes, M
- Tardieu, M
- Chelly, J
Producer: 20000829
In:
Human molecular genetics vol. 9
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23.
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The coupled atom transistor. [electronic resource] by
- Jehl, X
- Voisin, B
- Roche, B
- Dupont-Ferrier, E
- De Franceschi, S
- Sanquer, M
- Cobian, M
- Niquet, Y-M
- Sklénard, B
- Cueto, O
- Wacquez, R
- Vinet, M
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In:
Journal of physics. Condensed matter : an Institute of Physics journal vol. 27
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24.
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Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardation. [electronic resource] by
- Billuart, P
- Vinet, M C
- des Portes, V
- Llense, S
- Richard, L
- Moutard, M L
- Recan, D
- Brüls, T
- Bienvenu, T
- Kahn, A
- Beldjord, C
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Producer: 19970116
In:
Human molecular genetics vol. 5
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25.
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Gate-reflectometry dispersive readout and coherent control of a spin qubit in silicon. [electronic resource] by
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- Hutin, L
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- Meunier, T
- Sanquer, M
- Jehl, X
- Maurand, R
- De Franceschi, S
Publication details: Nature communications Jul 2019
In:
Nature communications vol. 10
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26.
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X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pter. [electronic resource] by
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- Bachner, L
- Brüls, T
- Beldjord, C
- Billuart, P
- Soufir, N
- Bienvenu, T
- Vinet, M C
- Malaspina, E
- Marchiani, V
- Bertini, E
- Kahn, A
- Franzoni, E
- Chelly, J
Producer: 19961120
In:
American journal of medical genetics vol. 64
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27.
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A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. [electronic resource] by
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- Pinard, J M
- Billuart, P
- Vinet, M C
- Koulakoff, A
- Carrié, A
- Gelot, A
- Dupuis, E
- Motte, J
- Berwald-Netter, Y
- Catala, M
- Kahn, A
- Beldjord, C
- Chelly, J
Producer: 19980316
In:
Cell vol. 92
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28.
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Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons. [electronic resource] by
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- Koulakoff, A
- Boucher, D
- Chafey, P
- Schaar, B
- Vinet, M C
- Friocourt, G
- McDonnell, N
- Reiner, O
- Kahn, A
- McConnell, S K
- Berwald-Netter, Y
- Denoulet, P
- Chelly, J
Producer: 19991028
In:
Neuron vol. 23
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29.
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Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia. [electronic resource] by
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- Ramser, J
- Francis, F
- Vinet, M C
- Rider, S
- Sudbrak, R
- Riesselman, L
- Yaspo, M L
- Reinhardt, R
- Monaco, A P
- Ross, F
- Kahn, A
- Kearney, L
- Buckle, V
- Chelly, J
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In:
Genomics vol. 64
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30.
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Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation. [electronic resource] by
- Billuart, P
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- Ronce, N
- des Portes, V
- Vinet, M C
- Zemni, R
- Roest Crollius, H
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- Fauchereau, F
- Cherry, M
- Briault, S
- Hamel, B
- Fryns, J P
- Beldjord, C
- Kahn, A
- Moraine, C
- Chelly, J
Producer: 19980518
In:
Nature vol. 392
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31.
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Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor. [electronic resource] by
- Bienvenu, T
- des Portes, V
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- McDonell, N
- Billuart, P
- Carrié, A
- Vinet, M C
- Couvert, P
- Toniolo, D
- Ropers, H H
- Moraine, C
- van Bokhoven, H
- Fryns, J P
- Kahn, A
- Beldjord, C
- Chelly, J
Producer: 19980909
In:
Human molecular genetics vol. 7
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32.
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Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22. [electronic resource] by
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- Pinard, J M
- Smadja, D
- Motte, J
- Boespflüg-Tanguy, O
- Moutard, M L
- Desguerre, I
- Billuart, P
- Carrie, A
- Bienvenu, T
- Vinet, M C
- Bachner, L
- Beldjord, C
- Dulac, O
- Kahn, A
- Ponsot, G
- Chelly, J
Producer: 19970430
In:
Journal of medical genetics vol. 34
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33.
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Fast Gate-Based Readout of Silicon Quantum Dots Using Josephson Parametric Amplification. [electronic resource] by
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- Ahmed, I
- Haigh, J A
- Hutin, L
- Bertrand, B
- Barraud, S
- Vinet, M
- Lee, C-M
- Stelmashenko, N
- Robinson, J W A
- Qiu, J Y
- Hacohen-Gourgy, S
- Siddiqi, I
- Gonzalez-Zalba, M F
- Morton, J J L
Publication details: Physical review letters Feb 2020
In:
Physical review letters vol. 124
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34.
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[Economic and organizational impact of the use of a disposable sheath with a flexible cystoscope]. [electronic resource] by
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- Ruffion, A
- Lechevallier, E
- Devonec, M
- Paparel, P
- Champetier, D
- Vinet, M
- Adam, E
- Briant, P E
- De Vendin, C
- Coulange, C
- Delaporte, V
- Gaillet, S
- Faïs, P O
- Monges, A
- Arnoux, V
- Armoiry, X
- Gardes, S
- Bin, S
- Karsenty, G
Producer: 20130930
In:
Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie vol. 23
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35.
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A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation. [electronic resource] by
- Carrié, A
- Jun, L
- Bienvenu, T
- Vinet, M C
- McDonell, N
- Couvert, P
- Zemni, R
- Cardona, A
- Van Buggenhout, G
- Frints, S
- Hamel, B
- Moraine, C
- Ropers, H H
- Strom, T
- Howell, G R
- Whittaker, A
- Ross, M T
- Kahn, A
- Fryns, J P
- Beldjord, C
- Marynen, P
- Chelly, J
Producer: 19990923
In:
Nature genetics vol. 23
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36.
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A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. [electronic resource] by
- Zemni, R
- Bienvenu, T
- Vinet, M C
- Sefiani, A
- Carrié, A
- Billuart, P
- McDonell, N
- Couvert, P
- Francis, F
- Chafey, P
- Fauchereau, F
- Friocourt, G
- des Portes, V
- Cardona, A
- Frints, S
- Meindl, A
- Brandau, O
- Ronce, N
- Moraine, C
- van Bokhoven, H
- Ropers, H H
- Sudbrak, R
- Kahn, A
- Fryns, J P
- Beldjord, C
- Chelly, J
Producer: 20000228
In:
Nature genetics vol. 24
Availability: No items available.
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