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Author/Creator Meire, Françoise

1. An Augmented ABCA4 Screen Targeting Noncoding Regions Reveals a Deep Intronic Founder Variant in Belgian Stargardt Patients. Issue 1 (January 2015)

Authors:
Bauwens, Miriam; De Zaeytijd, Julie; Weisschuh, Nicole; Kohl, Susanne; Meire, Françoise; Dahan, Karin; Depasse, Fanny; De Jaegere, Sarah; De Ravel, Thomy; De Rademaeker, Marjan; Loeys, Bart; Coppieters, Frauke; Leroy, Bart P.; De Baere, Elfride
Journal:
Human mutation
Issue:
Volume 36:Issue 1(2015:Jan.)
Page Start:
39
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Hidden Genetic Variation in LCA9‐Associated Congenital Blindness Explained by 5′UTR Mutations and Copy‐Number Variations of NMNAT1. Issue 12 (1st October 2015)

Authors:
Coppieters, Frauke; Todeschini, Anne Laure; Fujimaki, Takuro; Baert, Annelot; De Bruyne, Marieke; Van Cauwenbergh, Caroline; Verdin, Hannah; Bauwens, Miriam; Ongenaert, Maté; Kondo, Mineo; Meire, Françoise; Murakami, Akira; Veitia, Reiner A.; Leroy, Bart P.; De Baere, Elfride
Journal:
Human mutation
Issue:
Volume 36:Issue 12(2015:Dec.)
Page Start:
1188
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Uncommon Leber "Plus" Disease Associated With Mitochondrial Mutation m.11778G>A in a Premature Child. (August 2014)

Authors:
Paquay, Stéphanie; Benoit, Valérie; Wetzburger, Catherine; Cordonnier, Monique; Meire, Françoise; Charon, Anne; Roland, Dominique; Coster, Rudy Van; Nassogne, Marie-Cécile; Maystadt, Isabelle
Other Names:
Majnemer Annette guest-editor.
Journal:
Journal of child neurology
Issue:
Volume 29:Number 8(2014:Aug.)
Page Start:
NP18
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗