The clinical phenotype of children with Fanconi anemia caused by biallelic FANCD1/BRCA2 mutations.
Myers K; Davies SM; Harris RE; Spunt SL; Smolarek T; Zimmerman S; McMasters R; Wagner L; Mueller R; Auerbach AD; Mehta PA; Pediatric Blood & Cancer, 2012, vol. 58, issue 3, p 462, ISSN 15455017. ISBN 15455017.

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