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Fig. 3 | Molecular Cytogenetics

Fig. 3

From: 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 phenotype

Fig. 3

Schematic representation of the genomic region harboring FOXF1, FOXC2, and FOXL1 showed the extent and primary gene content of the regions deleted in 11 cases, according to different versions of the genome map from UCSC Genome Browser Home: a cases from C1 to C8 were plotted with HG18; b cases from 9 to 11 with HG19

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Molecular Cytogenetics

ISSN: 1755-8166