TY - JOUR
T1 - Correction to: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature (Genetics in Medicine, (2018), 10.1038/s41436-018-0339-3)
AU - Borgatti, Renato
AU - Nava, Consuelo Rubina
AU - Piard, Juliette
AU - Hawkes, Lara
AU - Milh, Mathieu
AU - Villard, Laurent
AU - Romaniello, Romina
AU - Fradin, Melanie
AU - Capri, Yline
AU - Héron, Delphine
AU - Nougues, Marie-Christine
AU - Nava, Caroline
AU - Arsene, Oana Tarta
AU - Shears, Debbie
AU - Taylor, John
AU - Pagnamenta, Alistair
AU - Taylor, Jenny C
AU - Sogawa, Yoshimi
AU - Johnson, Diana
AU - Firth, Helen
AU - Vasudevan, Pradeep
AU - Jones, Gabriela
AU - Nguyen-Morel, Marie-Ange
AU - Busa, Tiffany
AU - Roubertie, Agathe
AU - Van Den Born, Myrthe
AU - Brischoux-Boucher, Elise
AU - Koenig, Michel
AU - Mignot, Cyril
AU - Kini, Usha
AU - Philippe, Christophe
PY - 2019
Y1 - 2019
N2 - The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature
AB - The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature
KW - WWOX-related disorders
KW - WWOX-related disorders
UR - http://hdl.handle.net/10807/134378
UR - https://www.scopus.com/inward/record.uri?eid=2-s2.0-85061972303&doi=10.1038%2fs41436-019-0460-y&partnerid=40&md5=5678343063e8787116f97447dc860a8b
U2 - 10.1038/s41436-019-0460-y
DO - 10.1038/s41436-019-0460-y
M3 - Article
VL - 2019
SP - 1-1+1
JO - Genetics in Medicine
JF - Genetics in Medicine
SN - 1098-3600
ER -