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A case of neonatal galactosemia presenting with rare hematologic problems: factor V deficiency and hemophagocytic lymphohistiocytosis

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A case of neonatal galactosemia presenting with rare hematologic problems: factor V deficiency and hemophagocytic lymphohistiocytosis

01 Ocak 2026 Makale Google Scholar

Atıf kopyala

P. M. ALBAYRAK (2026). A case of neonatal galactosemia presenting with rare hematologic problems: factor V deficiency and hemophagocytic lymphohistiocytosis. *The Turkish Journal of Pediatrics, 1-5, 2026*.

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Dergi The Turkish Journal of Pediatrics, 1-5, 2026
Veri tabanı Google Scholar
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Atıf verisi 13 Kasım 2026 tarihinde güncellendi.

Ş Toprak, Ü Koral, S Alan, HF Gülerman, M Albayrak | The Turkish Journal of Pediatrics, 1-5, 2026

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