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. 2021 Oct 29;12:750110. doi: 10.3389/fgene.2021.750110

FIGURE 1.

FIGURE 1

Pedigree of the Czech family with ATS-ID syndrome. Proband (IV-1) and his maternal uncle (III-5) have hemizygous deletion in Xq22.3; the mother (III-4) and grandmother (II-4) are heterozygous for deletion Xq22.3.