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Valérie Charraud
Valérie Charraud
University of Poitiers
Genetics
Biology
Osteogenesis imperfecta
DLX3
Candidate gene
2
Papers
22
Citations
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Osteogenesis imperfecta, tricho-dento-osseous syndrome and intellectual disability: A familial case with 17q21.33-q22 (COL1A1 and DLX3) deletion and 7q32.3-q33 duplication resulting from a reciprocal interchromosomal insertion
2013
American Journal of Medical Genetics Part A
Radu Harbuz
Frédéric Bilan
Dominique Couet
Valérie Charraud
Alain Kitzis
Brigitte Gilbert-Dussardier
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Citations (9)
Complete screening of 50 patients with CHARGE syndrome for anomalies in the CHD7 gene using a denaturing high-performance liquid chromatography-based protocol: new guidelines and a proposal for routine diagnosis.
2012
The Journal of Molecular Diagnostics
Frédéric Bilan
Marine Legendre
Valérie Charraud
Barbara Manière
Dominique Couet
Brigitte Gilbert-Dussardier
Alain Kitzis
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Citations (13)
1