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Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant.
Ital J Pediatr. 2017 Nov 3;43(1):100. doi: 10.1186/s13052-017-0418-0.
Ital J Pediatr. 2017.
PMID: 29100554
Free PMC article.
Review.
Recommendations for neonatologists and pediatricians working in first level birthing centers on the first communication of genetic disease and malformation syndrome diagnosis: consensus issued by 6 Italian scientific societies and 4 parents' associations.
Serra G, Memo L, Coscia A, Giuffré M, Iuculano A, Lanna M, Valentini D, Contardi A, Filippeschi S, Frusca T, Mosca F, Ramenghi LA, Romano C, Scopinaro A, Villani A, Zampino G, Corsello G; their respective Scientific Societies and Parents’ Associations.
Serra G, et al.
Ital J Pediatr. 2021 Apr 19;47(1):94. doi: 10.1186/s13052-021-01044-1.
Ital J Pediatr. 2021.
PMID: 33874990
Free PMC article.
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