Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes
Crossref DOI link: https://0-doi-org.brum.beds.ac.uk/10.1186/s12885-015-1549-6
Published Online: 2015-07-23
Published Print: 2015-12
Update policy: https://0-doi-org.brum.beds.ac.uk/10.1007/springer_crossmark_policy
Spinella, Jean-François
Healy, Jasmine
Saillour, Virginie
Richer, Chantal
Cassart, Pauline
Ouimet, Manon
Sinnett, Daniel
License valid from 2015-07-23
Article History
Received: 2 December 2014
Accepted: 14 July 2015
First Online: 23 July 2015