Items where Author is "Mancini, Grazia Maria Simonetta"

Article

Brock, Stefanie and Laquerriere, Annie and Marguet, Florent and Myers, Scott J. and Hongjie, Yuan and Baralle, Diana and Vanderhasselt, Tim and Stouffs, Katrien and Keymolen, Kathelijn and Kim, Sukhan and Allen, James and Shaulsky, Gil and Chelly, Jamel and Marcorelle, Pascale and Aziza, Jacqueline and Villard, Laurent and Sacaze, Elise and de Wit, Marie C. Y. and Wilke, Martina and Mancini, Grazia Maria Simonetta and Hehr, Ute and Lim, Derek and Mansour, Sahar and Traynelis, Stephen F. and Beneteau, Claire and Denis-Musquer, Marie and Jansen, Anna C. and Fry, Andrew E. and Bahi-Buisson, Nadia (2023) Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B. JOURNAL OF MEDICAL GENETICS, 60 (2). pp. 183-192. ISSN 0022-2593, 1468-6244

Brock, Stefanie and Vanderhasselt, Tim and Vermaning, Sietske and Keymolen, Kathelijn and Regal, Luc and Romaniello, Romina and Wieczorek, Dagmar and Storm, Tim Matthias and Schaeferhoff, Karin and Hehr, Ute and Kuechler, Alma and Kraegeloh-Mann, Ingeborg and Haack, Tobias B. and Kasteleijn, Esmee and Schot, Rachel and Mancini, Grazia Maria Simonetta and Webster, Richard and Mohammad, Shekeeb and Leventer, Richard J. and Mirzaa, Ghayda and Dobyns, William B. and Bahi-Buisson, Nadia and Meuwissen, Marije and Jansen, Anna C. and Stouffs, Katrien (2021) Defining the phenotypical spectrum associated with variants in TUBB2A. JOURNAL OF MEDICAL GENETICS, 58 (1). pp. 33-40. ISSN 0022-2593, 1468-6244