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

E.A. Colombo; H. Mutlu-Albayrak; Y. Shafeghati; M. Balasar; J. Piard; D. Gentilini; A.M. Di Blasio; C. Gervasini; L. Van Maldergem; L. Larizza

doi:10.3389/fped.2019.00210

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

E.A. Colombo, H. Mutlu-Albayrak, Y. Shafeghati, M. Balasar, J. Piard, D. Gentilini, A.M. Di Blasio, C. Gervasini, L. Van Maldergem, L. Larizza

Research output: Contribution to journal › Article

Original language	Italian
Journal	Frontiers in Pediatrics
Volume	7
Issue number	MAY
DOIs	https://doi.org/10.3389/fped.2019.00210
Publication status	Published - 2019

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10.3389/fped.2019.00210

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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. (2019). Phenotypic overlap of Roberts and Baller-Gerold syndromes in two patients with craniosynostosis, limb reductions, and ESCO2 mutations. Frontiers in Pediatrics, 7(MAY). https://doi.org/10.3389/fped.2019.00210

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

In: Frontiers in Pediatrics, Vol. 7, No. MAY, 2019.

Research output: Contribution to journal › Article

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author = "E.A. Colombo and H. Mutlu-Albayrak and Y. Shafeghati and M. Balasar and J. Piard and D. Gentilini and {Di Blasio}, A.M. and C. Gervasini and {Van Maldergem}, L. and L. Larizza",

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AU - Colombo, E.A.

AU - Mutlu-Albayrak, H.

AU - Shafeghati, Y.

AU - Balasar, M.

AU - Piard, J.

AU - Gentilini, D.

AU - Di Blasio, A.M.

AU - Gervasini, C.

AU - Van Maldergem, L.

AU - Larizza, L.

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