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Levy, Brian J. [Author] ; Bozon, Nicole [Other]

Nine verse sermons by Nicholas Bozon : the art of an Anglo-Norman poet and preacher

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Oxford: The Soc. for the Study of Mediaeval Languages and Literature, 1981

Published in: Medium aevum <Oxford> / Monographs ; 1011
Bozon, Nicole [Author] ; Vising, Johan [Editor]

Deux poèmes de Nicholas Bozon

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Göteborg: Elander, 1919

Published in: Göteborgs Högskola: Göteborgs Högskolas årsskrift ; 25,3
Bozon, Nicole [Author] ; Thorn, A. Chr [Editor]

Les proverbes de bon enseignement de Nicole Bozon

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Lund: Gleerup, 1921 ; Leipzig: Harrassowitz, 1921

Published in: Lunds universitet: Lunds Universitets årsskrift / 1 ; 1017,4
Verot, Lucie; Alloisio, Nicole; Morlé, Laurette; Bozon, Muriel; Touraine, Renaud; Plauchu, Henri; Edery, Patrick

Localization of a non‐syndromic X‐linked mental retardation gene (MRX80) to Xq22‐q24

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Wiley, 2003

Published in: American Journal of Medical Genetics Part A, 122A (2003) 1, Seite 37-41
Faure, Alexis; Es-seddiqi, Mouna; Brown, Bruce L.; Nguyen, Hoa P.; Riess, Olaf; von Hörsten, Stephan; Le Blanc, Pascale; Desvignes, Nathalie; Bozon, Bruno; El Massioui, Nicole; Doyère, Valérie

Modified impact of emotion on temporal discrimination in a transgenic rat model of Huntington disease

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Frontiers Media SA, 2013

Published in: Frontiers in Behavioral Neuroscience, 7 (2013)
Alloisio, Nicole; Morlé, Laurette; Bozon, Muriel; Godet, Jacqueline; Verhoeven, Kristien; Van Camp, Guy; Plauchu, Henri; Muller, Philippe; Collet, Lionel; Lina-Granade, Geneviève

Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss

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Springer Science and Business Media LLC, 1999

Published in: European Journal of Human Genetics, 7 (1999) 2, Seite 255-258
Maillet, Philippe; Venezia, Nicole Dalla; Lorenzo, Fr�d�ric; Morini�re, Madeleine; Bozon, Muriel; No�l, Bernard; Delaunay, Jean; Baklouti, Faouzi

A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon

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Hindawi Limited, 1999

Published in: Human Mutation, 14 (1999) 2, Seite 145-155
Zech, Jean-Christophe; Morlé, Laurette; Vincent, Pascale; Alloisio, Nicole; Bozon, Muriel; Gonnet, Colette; Milazzo, Solange; Grange, Jean-Daniel; Trepsat, Christiane; Godet, Jacqueline; Plauchu, Henri

Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14

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Springer Science and Business Media LLC, 1999

Published in: Graefe's Archive for Clinical and Experimental Ophthalmology, 237 (1999) 5, Seite 387-393
Ménard, Marie; Costechareyre, Clélia; Coelho-Aguiar, Juliana M.; Jarrosson-Wuilleme, Loraine; Rama, Nicolas; Blachier, Jonathan; Kindbeiter, Karine; Bozon, Muriel; Cabrera, Jorge R.; Dupin, Elisabeth; Le Douarin, Nicole; Mehlen, Patrick; Tauszig-Delamasure, Servane

The dependence receptor TrkC regulates the number of sensory neurons during DRG development

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Elsevier BV, 2018

Published in: Developmental Biology, 442 (2018) 2, Seite 249-261
Feldmann, Delphine; Couderc, Remy; Audrezet, Marie-Pierre; Ferec, Claude; Bienvenu, Thierry; Desgeorges, Marie; Claustres, Mireille; Mittre, Herv�; Blayau, Martine; Bozon, Dominique; Malinge, Marie-Claire; Monnier, Nicole; Bonnefont, Jean-Paul; Iron, Albert; Bieth, Eric; Dumur, Viviane; Clavel, Christine; Cazeneuve, C�cile; Girodon, Emmanuelle

CFTR genotypes in patients with normal or borderline sweat chloride levels

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Hindawi Limited, 2003

Published in: Human Mutation, 22 (2003) 4, Seite 340-340
Claustres, Mireille; Guittard, Caroline; Bozon, Dominique; Chevalier, Fran�oise; Verlingue, Claudine; Ferec, Claude; Girodon, Emanuelle; Cazeneuve, C�cile; Bienvenu, Thierry; Lalau, Guy; Dumur, Viviane; Feldmann, Delphine; Bieth, Eric; Blayau, Martine; Clavel, Christine; Creveaux, Isabelle; Malinge, Marie-Claire; Monnier, Nicole; Malzac, Perrine; Mittre, Herv�; Chomel, Jean-Claude; Bonnefont, Jean-Paul; Iron, Albert; Chery, Mich�le;

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

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Hindawi Limited, 2000

Published in: Human Mutation, 16 (2000) 2, Seite 143-156
Szot, Justin O.; Cuny, Hartmut; Martin, Ella M.M.A.; Sheng, Delicia Z.; Iyer, Kavitha; Portelli, Stephanie; Nguyen, Vivien; Gereis, Jessica M.; Alankarage, Dimuthu; Chitayat, David; Chong, Karen; Wentzensen, Ingrid M.; Vincent-Delormé, Catherine; Lermine, Alban; Burkitt-Wright, Emma; Ji, Weizhen; Jeffries, Lauren; Pais, Lynn S.; Tan, Tiong Y.; Pitt, James; Wise, Cheryl A.; Wright, Helen; Andrews, Israel D.; Pruniski, Brianna; [...]

A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder

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American Society for Clinical Investigation, 2024

Published in: Journal of Clinical Investigation, 134 (2024) 4

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