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Fig. 1 | BMC Cancer

Fig. 1

From: Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes

Fig. 1

Family pedigree. The family is of self-reported Moroccan origin and consists of five siblings, including two non-twinned brothers diagnosed with pre-B acute lymphoblastic leukemia (A and B) as well as two healthy females and one healthy male. Affected probands are represented by the shaded squares; cousins with poly-malformation syndrome are represented by half-shaded circles. Sequenced individuals are identified by an asterisk

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BMC Cancer

ISSN: 1471-2407

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