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Author/Creator Devisme, Louise

12. Possible association between complex congenital heart defects and 11p15 hypomethylation in three patients with severe Silver–Russell syndrome1. Issue 3 (7th February 2013)

Authors:
Ghanim, Mustafa; Rossignol, Sylvie; Delobel, Bruno; Irving, Melita; Miller, Owen; Devisme, Louise; Plennevaux, Jean‐Louis; Lucidarme‐Rossi, Sophie; Manouvrier, Sylvie; Salah, Azzi; Chivu, Olimpia; Netchine, Irène; Vincent‐Delorme, Catherine
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 3(2013:Mar.)
Page Start:
572
Record Type:
Journal Article
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15. TAR syndrome: Clinical and molecular characterization of a cohort of 26 patients and description of novel noncoding variants of RBM8A. Issue 7 (6th April 2020)

Authors:
Boussion, Simon; Escande, Fabienne; Jourdain, Anne‐Sophie; Smol, Thomas; Brunelle, Perrine; Duhamel, Céline; Alembik, Yves; Attié‐Bitach, Tania; Baujat, Geneviève; Bazin, Anne; Bonnière, Maryse; Carassou, Philippe; Carles, Dominique; Devisme, Louise; Goizet, Cyril; Goldenberg, Alice; Grotto, Sara...
Journal:
Human mutation
Issue:
Volume 41:Issue 7(2020)
Page Start:
1220
Record Type:
Journal Article
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16. The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome. Issue 4 (13th July 2021)

Authors:
Ghesh, Leïla; Musquer, Marie Denis; Devisme, Louise; Stichelbout, Morgane; Boutaud, Lucile; Elkhartoufi, Nadia; Vaast, Pascal; Boute, Odile; Riteau, Anne‐Sophie; Le Vaillant, Claudine; Winer, Norbert; Joubert, Madeleine; Bezieau, Stéphane; Thomas, Sophie; Attie‐Bitach, Tania; Beneteau, Claire
Journal:
Clinical genetics
Issue:
Volume 100:Issue 4(2021)
Page Start:
462
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗