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Date 2016 Author/Creator Giraud, Mathilde

1. A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture. Issue 11 (March 2016)

Authors:
Veyradier, Agnès; Boisseau, Pierre; Fressinaud, Edith; Caron, Claudine; Ternisien, Catherine; Giraud, Mathilde; Zawadzki, Christophe; Trossaert, Marc; Itzhar-Baïkian, Nathalie; Dreyfus, Marie; d'Oiron, Roseline; Borel-Derlon, Annie; Susen, Sophie; Bezieau, Stéphane; Denis, Cécile V.; Goudemand, J...
Editors:
Marchi., Rita
Journal:
Medicine
Issue:
Volume 95:Issue 11(2016)
Page Start:
e3038
Record Type:
Journal Article
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3. Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next‐generation sequencing. Issue 2 (21st November 2016)

Authors:
Baurand, Amandine; Falcon‐Eicher, Sylvie; Laurent, Gabriel; Villain, Elisabeth; Bonnet, Caroline; Thauvin‐Robinet, Christel; Jacquot, Caroline; Eicher, Jean‐Christophe; Gourraud, Jean‐Baptiste; Schmitt, Sébastien; Bézieau, Stéphane; Giraud, Mathilde; Dumont, Solenne; Kuentz, Paul; Probst, Vincent...
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 2(2017)
Page Start:
531
Record Type:
Journal Article
View Content:
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