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Faruk Incecik
ORCID
Publication Activity (10 Years)
Years Active: 2019-2019
Publications (10 Years): 1
Top Topics
Low Dose
Soft Tissue
Subarachnoid Hemorrhage
Genome Wide Analysis
Top Venues
Pediatric hematology and oncology
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This page only lists publications with an associated author ORCID identifier.
Publications
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Rabia Miray Kisla Ekinci
,
Sibel Balcı
,
Serdar Ceylaner
,
Hatice Ilgen Sasmaz
,
Goksel Leblebisatan
,
Faruk Incecik
,
Mustafa Yilmaz
A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia.
Pediatric hematology and oncology
36 (6) (2019)