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Keywords: RFWD3
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Journal Articles
Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature
Available to Purchase
Journal:
Molecular Syndromology
Mol Syndromol (2023) 14 (6): 509–515.
Published Online: 04 August 2023
...Sinem Kocagil; İkbal Nur Şafak; Elif Saraç; Can Aydın; Sevilhan Artan; Birgül Kırel Introduction: Fanconi anemia (FA) is a heterogeneous genetic disorder that is characterized by progressive bone marrow failure, congenital malformations, predisposition to malignancy, and short stature. The RFWD3...
