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Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene

✍ Scribed by Eleanor S. Click; Barbara Cox; Susan B. Olson; Markus Grompe; Yassmine Akkari; Lisa A. Moreau; Akiko Shimamura; Darci L. Sternen; Yajuan J. Liu; Kathleen A. Leppig; Dana C. Matthews; Melissa A. Parisi

Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 990 KB
Volume: 155
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.34024

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