Atıf İçin Kopyala
Gozdasoglu S., Ertem M., Uysal Z., Babacan E., Yuksel M., Bokesoy I., ...Daha Fazla
TURKISH JOURNAL OF HEMATOLOGY, cilt.26, sa.3, ss.118-122, 2009 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
26
Sayı:
3
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Basım Tarihi:
2009
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Dergi Adı:
TURKISH JOURNAL OF HEMATOLOGY
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
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Sayfa Sayıları:
ss.118-122
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Anahtar Kelimeler:
Fanconi, acute myeloid leukemia, congenital abnormalities, diepoxybutane, APLASTIC-ANEMIA, CANCER, CHILDHOOD, MUTATIONS, REGISTRY
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Ankara Üniversitesi Adresli:
Evet
Özet
Objective: Fanconi's anemia (FA) is an autosomal recessive disorder characterized by a progressive pancytopenia,variable congenital abnormalities and an increased risk for the development of acute myeloid leukemia (AML). The objective of this study is to evaluate AML in the patients with FA diagnosed and followed-up in the Department of Pediatric Hematology at Ankara University School of Medicine in the period between 1964-1995.