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A NEWBORN CASE OF INTESTINAL INFARCTION WITH HOMOZYGOUS MTHFR C677T AND HETEROZYGOUS OF FACTOR V LEIDEN G1691A, PAI-1 4G/5G MUTATIONS

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dc.creator Ayata, A.
dc.creator Duman, L.
dc.creator Sandal, G.
dc.date 2014-01-01T01:00:00Z
dc.date.accessioned 2021-12-03T12:02:37Z
dc.date.available 2021-12-03T12:02:37Z
dc.identifier cab2332b-636d-4190-9a8b-db1527ee7988
dc.identifier https://avesis.sdu.edu.tr/publication/details/cab2332b-636d-4190-9a8b-db1527ee7988/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/94878
dc.description
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title A NEWBORN CASE OF INTESTINAL INFARCTION WITH HOMOZYGOUS MTHFR C677T AND HETEROZYGOUS OF FACTOR V LEIDEN G1691A, PAI-1 4G/5G MUTATIONS
dc.type info:eu-repo/semantics/article


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