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701.
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704.
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705.
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Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case. [electronic resource] by
- Carré, Aurore
- Szinnai, Gabor
- Castanet, Mireille
- Sura-Trueba, Sylvia
- Tron, Elodie
- Broutin-L'Hermite, Isabelle
- Barat, Pascal
- Goizet, Cyril
- Lacombe, Didier
- Moutard, Marie-Laure
- Raybaud, Christine
- Raynaud-Ravni, Catherine
- Romana, Serge
- Ythier, Hubert
- Léger, Juliane
- Polak, Michel
Producer: 20090708
In:
Human molecular genetics vol. 18
Availability: No items available.
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706.
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707.
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The integrity of cholinergic basal forebrain neurons depends on expression of Nkx2-1. [electronic resource] by
- Magno, Lorenza
- Kretz, Oliver
- Bert, Bettina
- Ersözlü, Sara
- Vogt, Johannes
- Fink, Heidrun
- Kimura, Shioko
- Vogt, Angelika
- Monyer, Hannah
- Nitsch, Robert
- Naumann, Thomas
Producer: 20120404
In:
The European journal of neuroscience vol. 34
Availability: No items available.
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708.
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709.
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710.
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711.
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712.
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713.
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714.
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716.
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717.
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718.
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719.
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New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes. [electronic resource] by
- Devos, David
- Vuillaume, Isabelle
- de Becdelievre, Alix
- de Martinville, Berengère
- Dhaenens, Claire-Marie
- Cuvellier, Jean-Christophe
- Cuisset, Jean-Marie
- Vallée, Louis
- Lemaitre, Marie-Pierre
- Bourteel, Hélène
- Hachulla, Eric
- Wallaert, Benoit
- Destée, Alain
- Defebvre, Luc
- Sablonnière, Bernard
Producer: 20070220
In:
Movement disorders : official journal of the Movement Disorder Society vol. 21
Availability: No items available.
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720.
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