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Author/Creator Dard, Rodolphe

1. Clinical and neuroimaging findings in 33 patients with MCAP syndrome: A survey to evaluate relevant endpoints for future clinical trials. Issue 5 (20th January 2021)

Authors:
Garde, Aurore; Guibaud, Laurent; Goldenberg, Alice; Petit, Florence; Dard, Rodolphe; Roume, Joelle; Mazereeuw‐Hautier, Juliette; Chassaing, Nicolas; Lacombe, Didier; Morice‐Picard, Fanny; Toutain, Annick; Arpin, Stéphanie; Boccara, Olivia; Touraine, Renaud; Blanchet, Patricia; Coubes, Christine; ...
Journal:
Clinical genetics
Issue:
Volume 99:Issue 5(2021)
Page Start:
650
Record Type:
Journal Article
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2. DNA ligase IV deficiency: Immunoglobulin class deficiency depends on the genotype. Issue 3 (22nd February 2017)

Authors:
Dard, Rodolphe; Herve, Bérénice; Leblanc, Thierry; de Villartay, Jean‐Pierre; Collopy, Laura; Vulliami, Tom; Drunat, Severine; Gorde, Stephanie; Babik, Abel; Souchon, Pierre‐François; Agadr, Aomar; Abilkassem, Rachid; Elalloussi, Mustapha; Verloes, Alain; Doco‐Fenzy, Martine
Journal:
Pediatric allergy and immunology
Issue:
Volume 28:Issue 3(2017)
Page Start:
298
Record Type:
Journal Article
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3. Effects of the implementation of second-line prenatal cell-free DNA testing on termination of pregnancy in a French perinatal network. (December 2021)

Authors:
Duvillier, Clémence; Dard, Rodolphe; Hervé, Bérénice; Cohen, Camille; Vialard, François; Quibel, Thibaud
Journal:
European journal of obstetrics, gynecology, and reproductive biology
Issue:
Volume 267(2021)
Page Start:
36
Record Type:
Journal Article
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4. Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases. Issue 12 (22nd September 2022)

Authors:
Testard, Quentin; Vanhoye, Xavier; Yauy, Kevin; Naud, Marie-Emmanuelle; Vieville, Gaelle; Rousseau, Francis; Dauriat, Benjamin; Marquet, Valentine; Bourthoumieu, Sylvie; Geneviève, David; Gatinois, Vincent; Wells, Constance; Willems, Marjolaine; Coubes, Christine; Pinson, Lucile; Dard, Rodolphe; ...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 12(2022)
Page Start:
1234
Record Type:
Journal Article
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6. Toward clinical and molecular dissection of frontonasal dysplasia with facial skin polyps: From Pai syndrome to differential diagnosis through a series of 27 patients. Issue 7 (21st April 2022)

Authors:
Lehalle, Daphné; Bruel, Ange‐Line; Vitobello, Antonio; Denommé‐Pichon, Anne‐Sophie; Duffourd, Yannis; Assoum, Mirna; Amiel, Jeanne; Baujat, Geneviève; Bessieres, Bettina; Bigoni, Stefania; Burglen, Lydie; Captier, Guillaume; Dard, Rodolphe; Edery, Patrick; Fortunato, Fernanda; Geneviève, David; G...
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 7(2022)
Page Start:
2036
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗