Browsing by Author Messiaen, Ludwine M.
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) |
|---|---|---|
| 2-Jun-2014 | SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints | Vogt, Julia; Bengesser, Kathrin; Claes, Kathleen B. M.; Wimmer, Katharina; Mautner, Victor-Felix; van Minkelen, Rick; Legius, Eric; Brems, Hilde; Upadhyaya, Meena; Högel, Josef; Lázaro García, Conxi; Rosenbaum, Thorsten; Bammert, Simone; Messiaen, Ludwine M.; Cooper, David N.; Kehrer-Sawatzki, Hildegard |
| Aug-2015 | The Third International Meeting on Genetic Disorders in the RAS/MAPK Pathway: Toward a Therapeutic Approach | Korf, Bruce; Ahmadian, Reza; Allanson, Judith; Aoki, Yoko; Bakker, Annette; Burkitt Wright, Emma; Denger, Brian; Elgersma, Ype; Gelb, Bruce D.; Gripp, Karen W.; Kerr, Bronwyn; Kontaridis, Maria; Lázaro García, Conxi; Linardic, Corinne; Lozano Rubí, Raimundo; MacRae, Calum A.; Messiaen, Ludwine M.; Mulero Navarro, Sonia; Neel, Benjamin; Plotkin, Scott; Rauen, Katherine A.; Roberts, Amy; Silva, Alcino J.; Sittampalam, Sitta G.; Zhang, Chao; Schoyer, Lisa |
| 20-Apr-2021 | Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Evans, D. Gareth; Messiaen, Ludwine M.; Foulkes, William D.; Irving, Rachel E. A.; Murray, Alexandra J.; Perez-becerril, Cristina; Rivera, Barbara; McDonald McGinn, Donna M.; Stevenson, David A.; Smith, Miriam J. |