Search Results - D'haene, Barbara
- Showing 1 - 4 results of 4
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1
Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain by Verdin, Hannah, D'haene, Barbara, Beysen, Diane, Novikova, Yana, Menten, Björn, Sante, Tom, Lapunzina, Pablo, Nevado, Julian, Carvalho, Claudia M. B., Lupski, James R., De Baere, Elfride
Published 2013Text -
2
Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G) by Benayoun, Bérénice A., Caburet, Sandrine, Dipietromaria, Aurélie, Georges, Adrien, D'Haene, Barbara, Pandaranayaka, P. J. Eswari, L'Hôte, David, Todeschini, Anne-Laure, Krishnaswamy, Sankaran, Fellous, Marc, De Baere, Elfride, Veitia, Reiner A.
Published 2010Text -
3
Structural and numerical changes of chromosome X in patients with esophageal atresia by Brosens, Erwin, de Jong, Elisabeth M, Barakat, Tahsin Stefan, Eussen, Bert H, D'haene, Barbara, De Baere, Elfride, Verdin, Hannah, Poddighe, Pino J, Galjaard, Robert-Jan, Gribnau, Joost, Brooks, Alice S, Tibboel, Dick, de Klein, Annelies
Published 2014Text -
4
Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening by D'haene, Barbara, Attanasio, Catia, Beysen, Diane, Dostie, Josée, Lemire, Edmond, Bouchard, Philippe, Field, Michael, Jones, Kristie, Lorenz, Birgit, Menten, Björn, Buysse, Karen, Pattyn, Filip, Friedli, Marc, Ucla, Catherine, Rossier, Colette, Wyss, Carine, Speleman, Frank, De Paepe, Anne, Dekker, Job, Antonarakis, Stylianos E., De Baere, Elfride
Published 2009Text