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Page 1
Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the FGB Gene.
Pediatr Rep. 2021 Mar 1;13(1):113-117. doi: 10.3390/pediatric13010016.
Pediatr Rep. 2021.
PMID: 33804389
Free PMC article.
Successful staged repair of pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries in an extremely low birth weight infant.
Ide Y, Murata M, Tachi M, Ito H, Nagasawa M, Ishigaki M, Kim SH, Nii M, Tanaka Y, Sakamoto K.
Ide Y, et al. Among authors: nagasawa m.
Gen Thorac Cardiovasc Surg. 2020 Jun;68(6):637-640. doi: 10.1007/s11748-019-01148-w. Epub 2019 May 30.
Gen Thorac Cardiovasc Surg. 2020.
PMID: 31147961
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