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 › peer-review

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

Access to Document

10.3389/fped.2019.00210

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85067429566&doi=10.3389%2ffped.2019.00210&partnerID=40&md5=952ff4227952620ad1b611638824e1bc

Cite this

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

@article{51c0dbfa7cb3481c885b217ad7895214,

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

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",

note = "Export Date: 5 February 2020",

year = "2019",

doi = "10.3389/fped.2019.00210",

language = "Italian",

volume = "7",

journal = "Frontiers in Pediatrics",

issn = "2296-2360",

publisher = "Frontiers Media S. A.",

number = "MAY",

}

TY - JOUR

T1 - Phenotypic overlap of Roberts and Baller-Gerold syndromes in two patients with craniosynostosis, limb reductions, and ESCO2 mutations

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.

N1 - Export Date: 5 February 2020

PY - 2019

Y1 - 2019

U2 - 10.3389/fped.2019.00210

DO - 10.3389/fped.2019.00210

M3 - Articolo

VL - 7

JO - Frontiers in Pediatrics

JF - Frontiers in Pediatrics

SN - 2296-2360

IS - MAY

ER -