Molecular diagnosis of Fanconi anemia with next-generation sequencing in a case with subtle signs and a negative chromosomal breakage test

D. Aslan, N. Ameziane, J.P. de Winter

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)282-285
JournalTurkish Journal of Pediatrics
Volume57
Issue number3
Publication statusPublished - 2015

Cite this