Fig. 2From: Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotypeThe CNV-seq result of fetus showed a 2.12-Mb deletion in 16q24.1q24.2 (85220000-87340000)Back to article page