Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study-Reference-Cited by-同舟云学术

Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study

Published:2015-12 Issue: Volume:451 Page:39-45
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Carrera Paola^ORCID,Di Resta Chiara,Volonteri Chiara,Castiglioni Emanuela,Bonfiglio Silvia,Lazarevic Dejan,Cittaro Davide,Stupka Elia,Ferrari Maurizio,Somaschini Marco,Magaldi Rosario,Rinaldi Matteo,Maffei Gianfranco,Stronati Mauro,Tzialla Chryssoula,Borghesi Alessandro,Tagliabue Paolo,Fedeli Tiziana,Citterio Marco,Mosca Fabio,Colnaghi Mariarosa,Lavizzari Anna,Agosti Massimo,Francescato Gaia,Pomero Giulia,Dalmazzo Cristina,Boldrini Antonio,Scaramuzzo Rosa,Bertino Enrico,Borgione Silvia,Martano Claudio,Carnielli Virgilio,Nobile Stefano,Auriemma Antonietta,Bellan Cristina,Carrera Giuseppe,Zambetti Chiara,Pucello Riccardo,Palatta Sara

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference58 articles.

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4. Neonatal outcomes of extremely preterm infants from the NICHD Neonatal Research Network;Stoll;Pediatrics,2010

5. Pathogenesis and treatment of bronchopulmonary dysplasia;Gien;Curr Opin Pediatr,2011

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