1. 11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver–Russell Syndrome. Issue 1 (26th October 2016) Authors: Abi Habib, Walid; Brioude, Frederic; Azzi, Salah; Salem, Jennifer; Das Neves, Cristina; Personnier, Claire; Chantot‐Bastaraud, Sandra; Keren, Boris; Le Bouc, Yves; Harbison, Madeleine D.; Netchine, Irene Journal: Human mutation Issue: Volume 38:Issue 1(2017) Page Start: 105 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Comment on: Juvenile granulosa cell ovarian tumor in a child with Beckwith‐Wiedemann syndrome. Issue 8 (11th January 2017) Authors: Brioude, Frederic; Netchine, Irène Journal: Pediatric blood & cancer Issue: Volume 64:Issue 8(2017) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations. Issue 11 (6th August 2019) Authors: Cohen, Enzo; Belkacem, Sabrina; Fedala, Soumeya; Collot, Nathalie; Khallouf, Eliane; Dastot, Florence; Polak, Michel; Duquesnoy, Philippe; Brioude, Frederic; Rose, Sophie; Viot, Géraldine; Soleyan, Aude; Carel, Jean‐Claude; Sobrier, Marie‐Laure; Chanson, Philippe; Gatelais, Frédérique; Heinrichs,... Journal: Human mutation Issue: Volume 40:Issue 11(2019) Page Start: 2033 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cover Image, Volume 173A, Number 7, July 2017. Issue 7 (July 2017) Authors: Kalish, Jennifer M.; Biesecker, Leslie G.; Brioude, Frederic; Deardorff, Matthew A.; Di Cesare‐Merlone, Alessandra; Druley, Todd; Ferrero, Giovanni B.; Lapunzina, Pablo; Larizza, Lidia; Maas, Saskia; Macchiaiolo, Marina; Maher, Eamonn R.; Maitz, Silvia; Martinez‐Agosto, Julian A.; Mussa, Alessand... Journal: American journal of medical genetics Issue: Volume 173:Issue 7(2017) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Is Nephron Sparing Surgery Justified in Wilms Tumor With Beckwith–Wiedemann Syndrome or Isolated Hemihypertrophy?. Issue 9 (27th May 2016) Authors: Scalabre, Aurélien; Bergeron, Christophe; Brioude, Frederic; Dainese, Linda; Cropet, Claire; Coulomb L'hermine, Aurore; Pasqualini, Claudia; Auber, Frederic; Verschuur, Arnauld; Schleiermacher, Gudrun; Le Bouc, Yves; Audry, Georges; Irtan, Sabine Journal: Pediatric blood & cancer Issue: Volume 63:Issue 9(2016) Page Start: 1571 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization. Issue 9 (6th August 2015) Authors: Brioude, Frederic; Netchine, Irène; Praz, Francoise; Le Jule, Marilyne; Calmel, Claire; Lacombe, Didier; Edery, Patrick; Catala, Martin; Odent, Sylvie; Isidor, Bertrand; Lyonnet, Stanislas; Sigaudy, Sabine; Leheup, Bruno; Audebert‐Bellanger, Séverine; Burglen, Lydie; Giuliano, Fabienne; Alessandr... Journal: Human mutation Issue: Volume 36:Issue 9(2015:Sep.) Page Start: 894 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Nomenclature and definition in asymmetric regional body overgrowth. Issue 7 (5th May 2017) Authors: Kalish, Jennifer M.; Biesecker, Leslie G.; Brioude, Frederic; Deardorff, Matthew A.; Di Cesare‐Merlone, Alessandra; Druley, Todd; Ferrero, Giovanni B.; Lapunzina, Pablo; Larizza, Lidia; Maas, Saskia; Macchiaiolo, Marina; Maher, Eamonn R.; Maitz, Silvia; Martinez‐Agosto, Julian A.; Mussa, Alessand... Journal: American journal of medical genetics Issue: Volume 173:Issue 7(2017) Page Start: 1735 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗