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Phenotypic overlap of Roberts and Baller-Gerold syndromes in two patients with craniosynostosis, limb reductions, and ESCO2 mutations

Academic Article
Publication Date:
2019
Iris type:
1.1 Articolo in rivista
Keywords:
Baller-Gerold syndrome; Differential diagnosis; ESCO2; Genetic counseling; Patient management; RECQL4; Roberts syndrome
List of contributors:
Colombo, E. A.; Mutlu-Albayrak, H.; Shafeghati, Y.; Balasar, M.; Piard, J.; Gentilini, D.; Di Blasio, A. M.; Gervasini, C.; Van Maldergem, L.; Larizza, L.
Authors of the University:
GENTILINI DAVIDE
LARIZZA DANIELA
Handle:
https://iris.unipv.it/handle/11571/1282487
Published in:
FRONTIERS IN PEDIATRICS
Journal
  • Overview

Overview

URL

https://www.frontiersin.org/journals/pediatrics
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