Sökresultat - D'Haene, Barbara

Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain av 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

Hämta fulltext Hämta fulltext Hämta fulltext

Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G) av 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.

Hämta fulltext Hämta fulltext Hämta fulltext

Structural and numerical changes of chromosome X in patients with esophageal atresia av 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

Hämta fulltext Hämta fulltext Hämta fulltext

Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening av 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

Hämta fulltext Hämta fulltext Hämta fulltext