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Fig. 2 | BMC Medical Genetics

Fig. 2

From: A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosis

Fig. 2

CGHa analysis. Panel a, CGH signals of patient’s chromosome 16. The deleted region is highlighted by a brown area. Panel b, chromosome 16 region containing the deletion. The deleted region is shown in red. Positions of FOX genes are shown in black. Positions of microsatellites LINC01081 and LINC01082 utilized for analysis are shown in green. Location of genes utilized for quantitative PCR are shown in blue. Base-pairs are numbered according to hg19

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