Fanconi anemia‐like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene
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M. Grompe | K. Leppig | M. Parisi | A. Shimamura | S. Olson | B. Cox | L. Moreau | Y. Akkari | Yajuan J. Liu | E. Click | D. Matthews | D. Sternen