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Author/Creator David, Véronique

1. Ferroportin Diseases: Functional Studies, a Link Between Genetic and Clinical Phenotype. Issue 11 (11th September 2013)

Authors:
Détivaud, Lénaïck; Island, Marie‐Laure; Jouanolle, Anne‐Marie; Ropert, Martine; Bardou‐Jacquet, Edouard; Le Lan, Caroline; Mosser, Annick; Leroyer, Patricia; Deugnier, Yves; David, Véronique; Brissot, Pierre; Loréal, Olivier
Journal:
Human mutation
Issue:
Volume 34:Issue 11(2013:Nov.)
Page Start:
1529
Record Type:
Journal Article
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2. Ferroportin Diseases: Functional Studies, a Link Between Genetic and Clinical Phenotype. Issue 11 (11th September 2013)

Authors:
Détivaud, Lénaïck; Island, Marie‐Laure; Jouanolle, Anne‐Marie; Ropert, Martine; Bardou‐Jacquet, Edouard; Le Lan, Caroline; Mosser, Annick; Leroyer, Patricia; Deugnier, Yves; David, Véronique; Brissot, Pierre; Loréal, Olivier
Journal:
Human mutation
Issue:
Volume 34:Issue 11(2013:Nov.)
Page Start:
1529
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway. Issue 12 (23rd August 2016)

Authors:
Dubourg, Christèle; Carré, Wilfrid; Hamdi‐Rozé, Houda; Mouden, Charlotte; Roume, Joëlle; Abdelmajid, Benmansour; Amram, Daniel; Baumann, Clarisse; Chassaing, Nicolas; Coubes, Christine; Faivre‐Olivier, Laurence; Ginglinger, Emmanuelle; Gonzales, Marie; Levy‐Mozziconacci, Annie; Lynch, Sally‐Ann; ...
Journal:
Human mutation
Issue:
Volume 37:Issue 12(2016)
Page Start:
1329
Record Type:
Journal Article
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4. New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases. Issue 11 (22nd September 2011)

Authors:
Mercier, Sandra; Dubourg, Christèle; Garcelon, Nicolas; Campillo-Gimenez, Boris; Gicquel, Isabelle; Belleguic, Marion; Ratié, Leslie; Pasquier, Laurent; Loget, Philippe; Bendavid, Claude; Jaillard, Sylvie; Rochard, Lucie; Quélin, Chloé; Dupé, Valérie; David, Véronique; Odent, Sylvie
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 11(2011)
Page Start:
752
Record Type:
Journal Article
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5. Recent advances in understanding inheritance of holoprosencephaly. Issue 2 (22nd May 2018)

Authors:
Dubourg, Christèle; Kim, Artem; Watrin, Erwan; de Tayrac, Marie; Odent, Sylvie; David, Véronique; Dupé, Valérie
Other Names:
Kruszka Paul S. guestEditor.; Solomon Benjamin D. guestEditor.; Muenke Maximilian guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 178:Issue 2(2018)
Page Start:
258
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗