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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 Web of Science

Atıf kopyala

P. S. ALAN (2026). A case of neonatal galactosemia presenting with rare hematologic problems: factor V deficiency and hemophagocytic lymphohistiocytosis. *TURKISH JOURNAL OF PEDIATRICS*, 68(4). https://doi.org/10.24953/turkjpediatr.2026.6374

Yayın bilgileri

Dergi TURKISH JOURNAL OF PEDIATRICS
Veri tabanı Web of Science
Kaynak WebOfScience
Cilt / Sayı 68 / 4

Atıf verisi 14 Kasım 2026 tarihinde güncellendi.

Toprak, Sule; Koral, Umran; Alan, Serdar; Gulerman, Hacer Fulya; Albayrak, Meryem | TURKISH JOURNAL OF PEDIATRICS

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Kaynak Atıf
Web of Science 0
Etkin 0

Yayın metrikleri (GS / WoS / Scopus)

0 Web of Science Atıf
Q3 JCR Quartile
0,326 SJR

Web of Science

Accession Number WOS:001875499300014

ISSN 0041-4301

JCR Quartile Q3 SCImago (field 2700, 2025)

Cilt / Sayı 68 / 4

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