Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations
成人期迈尔综合征:临床变异性和新出现的基因型-表型相关性
期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-024-01664-1
Vanbelleghem, Eva; Van Damme, Tim; Beyens, Aude; Symoens, Sofie; Claes, Kathleen; De Backer, Julie; Meerschaut, Ilse; Vanommeslaeghe, Floris; Delanghe, Sigurd E; van den Ende, Jenneke; Beyltjens, Tessi; Scimone, Eleanor R; Lindsay, Mark E; Schimmenti, Lisa A; Hinze, Alicia M; Dunn, Emily; Gomez-Ospina, Natalia; Vandernoot, Isabelle; Delguste, Thomas; Coppens, Sandra; Cormier-Daire, Valérie; Tartaglia, Marco; Garavelli, Livia; Shieh, Joseph; Demir, Şenol; Arslan Ateş, Esra; Zenker, Martin; Rohanizadegan, Mersedeh; Rivera-Cruz, Greysha; Douzgou, Sofia; Lin, Angela E; Callewaert, Bert