Francoise Charbonnier

Francoise Charbonnier

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Francoise Charbonnier

Francoise Charbonnier

Publications by authors named "Francoise Charbonnier"

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18Publications

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Efficiency of physiotherapy with Caycedian Sophrology on children with asthma: A randomized controlled trial.

Pediatr Pulmonol 2018 05 1;53(5):559-566. Epub 2018 Mar 1.

Department of Pediatric Cardiology and Pulmonology, University Hospital, Montpellier, France.

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http://dx.doi.org/10.1002/ppul.23982DOI Listing
May 2018

Familial solitary chondrosarcoma resulting from germline EXT2 mutation.

Genes Chromosomes Cancer 2017 02 25;56(2):128-134. Epub 2016 Oct 25.

Inserm U1079, Faculty of Medicine, UNIROUEN, Normandie Univ and Department of Genetics, Rouen University Hospital, Normandy Centre for Genomic and Personalized Medicine, Rouen, France.

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http://dx.doi.org/10.1002/gcc.22419DOI Listing
February 2017

Pitfalls in the use of DGV for CNV interpretation.

Am J Med Genet A 2011 Oct 9;155A(10):2593-6. Epub 2011 Sep 9.

Inserm U, Faculty of Medicine, Rouen University, France.

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http://dx.doi.org/10.1002/ajmg.a.34195DOI Listing
October 2011

Evaluation of Lynch syndrome modifier genes in 748 MMR mutation carriers.

Eur J Hum Genet 2011 Aug 16;19(8):887-92. Epub 2011 Mar 16.

Inserm U614, Faculty of Medicine, Institute for Biomedical Research and Innovation, University of Rouen, Rouen, France.

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http://dx.doi.org/10.1038/ejhg.2011.44DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172927PMC
August 2011

Prognostic value of circulating mutant DNA in unresectable metastatic colorectal cancer.

Ann Surg 2010 Feb;251(2):275-80

Inserm U614, Institute for Medical Research, Rouen Northwest Canceropole, France.

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http://dx.doi.org/10.1097/SLA.0b013e3181c35c87DOI Listing
February 2010

A large fraction of unclassified variants of the mismatch repair genes MLH1 and MSH2 is associated with splicing defects.

Hum Mutat 2008 Dec;29(12):1412-24

Inserm U614, Federate Institute for Multidisciplinary Research on Peptides, Faculty of Medicine, University of Rouen, Department of Genetics and Institute for Biomedical Research, Rouen University Hospital, Rouen, France.

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http://dx.doi.org/10.1002/humu.20796DOI Listing
December 2008

MSH2 in contrast to MLH1 and MSH6 is frequently inactivated by exonic and promoter rearrangements in hereditary nonpolyposis colorectal cancer.

Cancer Res 2002 Feb;62(3):848-53

Laboratoire de Génétique Moléculaire, CHU de Rouen et Institut National de la Santé et de la Recherche Médicale EMI 9906, Faculté de Médecine et de Pharmacie, IFRMP, 22 Boulevard de Gambetta, 76183 Rouen, France.

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February 2002