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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.
Puzzling (IRIDA-Like and Hemolytic) Anemia in a Child With Idiopathic Pulmonary Hemosiderosis.
Nishikado M, Awaguni H, Shinozuka J, Okumura K, Imashuku S.
Nishikado M, et al.
J Pediatr Hematol Oncol. 2022 May 1;44(4):191-193. doi: 10.1097/MPH.0000000000002385. Epub 2021 Dec 30.
J Pediatr Hematol Oncol. 2022.
PMID: 34966096
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