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had reviewed cases of congenital anomalies after in utero exposure to MTX and proved that some congenital anomalies such as microcephaly, craniosynostosis, tetralogy of Fallot, pulmonary valve atresia, limb reduction defects, and syndactyly were truly part of the fetal methotrexate syndrome [90]

It was found that this polymorphism did not increase the risk of melanoma (225)

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Ultimately, we measured substantial accumulation of the arachidonic acid peroxidation end product hydroxyeicosatetraenoic acid (HETE isomers) in RBCs stored in both E-Sol5 and to a lesser extent in SAGM, predominantly at +4 C (Fig

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