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Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith-Wiedemann syndrome as a sporadic adrenocortical tumor. [electronic resource] by
- H'mida Ben-Brahim, Dorra
- Hammami, Sabeur
- Haddaji Mastouri, Marwa
- Trabelsi, Saoussen
- Chourabi, Maroua
- Sassi, Sihem
- Mougou, Soumaya
- Gribaa, Moez
- Zakhama, Abdelfattah
- Guédiche, Mohamed Neji
- Saad, Ali
Producer: 20160303
In:
Applied & translational genomics vol. 4
Availability: No items available.
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Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA. [electronic resource] by
- Dimassi, Sarra
- Simonet, Thomas
- Labalme, Audrey
- Boutry-Kryza, Nadia
- Campan-Fournier, Amandine
- Lamy, Raphaelle
- Bardel, Claire
- Elsensohn, Mad-Hélénie
- Roucher-Boulez, Florence
- Chatron, Nicolas
- Putoux, Audrey
- de Bellescize, Julitta
- Ville, Dorothée
- Schaeffer, Laurent
- Roy, Pascal
- Mougou-Zerelli, Soumaya
- Saad, Ali
- Calender, Alain
- Sanlaville, Damien
- Lesca, Gaetan
Producer: 20160407
In:
Applied & translational genomics vol. 7
Availability: No items available.
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