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Page 1
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.
Carrera P, Di Resta C, Volonteri C, Castiglioni E, Bonfiglio S, Lazarevic D, Cittaro D, Stupka E, Ferrari M, Somaschini M; BPD and Genetics Study Group. Carrera P, et al. Clin Chim Acta. 2015 Dec 7;451(Pt A):39-45. doi: 10.1016/j.cca.2015.01.001. Epub 2015 Jan 8. Clin Chim Acta. 2015. PMID: 25578394
Screening patients affected by common variable immunodeficiency.
Masieri S, Orlando MP, Ciofalo A, Luzi G, Zambetti C, Filiaci F. Masieri S, et al. Among authors: zambetti c. Ann N Y Acad Sci. 1997 Dec 29;830:322-5. doi: 10.1111/j.1749-6632.1997.tb51904.x. Ann N Y Acad Sci. 1997. PMID: 9616692