Publications by authors named "Gregory Raux"

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A simple method for the routine detection of somatic quantitative genetic alterations in colorectal cancer.
Audrey Killian, Frédéric Di Fiore, Florence Le Pessot, France Blanchard, Aude Lamy, Grégory Raux

Gastroenterology· February 2007

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Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Grégory Raux, Emilie Bumsel, Bernadette Hecketsweiler, Therese van Amelsvoort, Janneke Zinkstok

Hum Mol Genet· January 2007

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Deleterious mutations in exon 1 of MECP2 in Rett syndrome.
Aline Quenard, Saliha Yilmaz, Hervé Fontaine, Thierry Bienvenu, Anne Moncla, Grégory Raux

Eur J Med Genet· September 2006

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Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients.
Gaëtan Lesca, Nelly Burnichon, Grégory Raux, Mario Tosi, Stéphane Pinson

Hum Mutat· June 2006

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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.
Anne Rovelet-Lecrux, Didier Hannequin, Gregory Raux, Nathalie Le Meur, Annie Laquerrière

Nat Genet· January 2006

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Acd, a peptidoglycan hydrolase of Clostridium difficile with N-acetylglucosaminidase activity.
Anne Dhalluin, Ingrid Bourgeois, Martine Pestel-Caron, Emilie Camiade, Gregory Raux

Microbiology (Reading)· July 2005

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A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.
Isabelle Le Ber, Maria Martinez, Dominique Campion, Annie Laquerrière, Christine Bétard, Gregory Raux

Brain· September 2004

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Analysis of the allele-specific expression of the mismatch repair gene MLH1 using a simple DHPLC-Based Method.
Isabelle Tournier, Grégory Raux, Fréderic Di Fiore, Isabelle Maréchal, Carole Leclerc

Hum Mutat· April 2004

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Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation.
Lucie Maréchal, Grégory Raux, Cécile Dumanchin, Guillaume Lefebvre, Emmanuelle Deslandre

Am J Med Genet B Neuropsychiatr Genet· May 2003

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Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene.
Gaëlle Bougeard, Laurence Brugières, Agnès Chompret, Paul Gesta, Françoise Charbonnier, Grégory Raux

Oncogene· February 2003

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PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.
Hélène Jacquet, Grégory Raux, Florence Thibaut, Bernadette Hecketsweiler, Emmanuelle Houy

Hum Mol Genet· September 2002

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