Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome

M. Cristina Digilio; Giulio Calcagni; Alessandro De Luca; Valentina Guida; Bruno Marino

doi:10.1016/j.jpeds.2019.10.050

Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome

M. Cristina Digilio, Giulio Calcagni, Alessandro De Luca, Valentina Guida, Bruno Marino

Research output: Contribution to journal › Letter

Original language	English
Pages (from-to)	263-264
Number of pages	2
Journal	Journal of Pediatrics
Volume	218
DOIs	https://doi.org/10.1016/j.jpeds.2019.10.050
Publication status	Published - Mar 2020

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health

Cite this

Digilio, M. C., Calcagni, G., De Luca, A., Guida, V., & Marino, B. (2020). Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome. Journal of Pediatrics, 218, 263-264. https://doi.org/10.1016/j.jpeds.2019.10.050

@article{4d4b26edd4ae4f188f53d7379b9d840e,

title = "Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome",

author = "Digilio, {M. Cristina} and Giulio Calcagni and {De Luca}, Alessandro and Valentina Guida and Bruno Marino",

year = "2020",

month = "3",

doi = "10.1016/j.jpeds.2019.10.050",

language = "English",

volume = "218",

pages = "263--264",

journal = "Journal of Pediatrics",

issn = "0022-3476",

publisher = "Mosby Inc.",

}

TY - JOUR

T1 - Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome

AU - Digilio, M. Cristina

AU - Calcagni, Giulio

AU - De Luca, Alessandro

AU - Guida, Valentina

AU - Marino, Bruno

PY - 2020/3

Y1 - 2020/3

UR - http://www.scopus.com/inward/record.url?scp=85079240522&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85079240522&partnerID=8YFLogxK

U2 - 10.1016/j.jpeds.2019.10.050

DO - 10.1016/j.jpeds.2019.10.050

M3 - Letter

C2 - 31843215

AN - SCOPUS:85079240522

VL - 218

SP - 263

EP - 264

JO - Journal of Pediatrics

JF - Journal of Pediatrics

SN - 0022-3476

ER -

Access to Document

10.1016/j.jpeds.2019.10.050

Projects

CASA SOLLIEVO SOFFERENZA - MECCANISMI PATOGENETICI E TERAPIA DELLE MALATTIE RARE

Project: Other project

Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome

ASJC Scopus subject areas

Cite this

Access to Document

Related content

Projects

CASA SOLLIEVO SOFFERENZA - MECCANISMI PATOGENETICI E TERAPIA DELLE MALATTIE RARE