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Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.
Carrera, Paola; Di Resta, Chiara; Volonteri, Chiara; Castiglioni, Emanuela; Bonfiglio, Silvia; Lazarevic, Dejan; Cittaro, Davide; Stupka, Elia; Ferrari, Maurizio; Somaschini, Marco.
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  • Carrera P; Unit of Genomics for Diagnosis of Human Pathologies, Division of Genetics and Cell Biology, IRCCS Ospedale San Raffaele, Milano, Italy; Laboratory of Clinical Molecular Biology, IRCCS Ospedale San Raffaele, Milano, Italy. Electronic address: carrera.paola@hsr.it.
  • Di Resta C; Unit of Genomics for Diagnosis of Human Pathologies, Division of Genetics and Cell Biology, IRCCS Ospedale San Raffaele, Milano, Italy.
  • Volonteri C; Vita-Salute San Raffaele University, Milano, Italy.
  • Castiglioni E; Unit of Genomics for Diagnosis of Human Pathologies, Division of Genetics and Cell Biology, IRCCS Ospedale San Raffaele, Milano, Italy.
  • Bonfiglio S; Centre for Translational Genomics and Bioinformatics, IRCCS Ospedale San Raffaele, Milano, Italy.
  • Lazarevic D; Centre for Translational Genomics and Bioinformatics, IRCCS Ospedale San Raffaele, Milano, Italy.
  • Cittaro D; Centre for Translational Genomics and Bioinformatics, IRCCS Ospedale San Raffaele, Milano, Italy.
  • Stupka E; Centre for Translational Genomics and Bioinformatics, IRCCS Ospedale San Raffaele, Milano, Italy.
  • Ferrari M; Unit of Genomics for Diagnosis of Human Pathologies, Division of Genetics and Cell Biology, IRCCS Ospedale San Raffaele, Milano, Italy; Laboratory of Clinical Molecular Biology, IRCCS Ospedale San Raffaele, Milano, Italy; Vita-Salute San Raffaele University, Milano, Italy.
  • Somaschini M; Unit of Genomics for Diagnosis of Human Pathologies, Division of Genetics and Cell Biology, IRCCS Ospedale San Raffaele, Milano, Italy.
Clin Chim Acta ; 451(Pt A): 39-45, 2015 Dec 07.
Article en En | MEDLINE | ID: mdl-25578394
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Displasia Broncopulmonar / Recien Nacido Prematuro / Exoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Infant / Newborn Idioma: En Revista: Clin Chim Acta Año: 2015 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Displasia Broncopulmonar / Recien Nacido Prematuro / Exoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans / Infant / Newborn Idioma: En Revista: Clin Chim Acta Año: 2015 Tipo del documento: Article