Fig. 1From: Nance-Horan Syndrome: characterization of dental, clinical and molecular features in three new families(a) Pedigrees of three NHS families. Probands are indicated by arrows. Affected individuals are indicated by filled-in symbols. Obligate carriers are represented by a central black dot. (b) Ideogram of X chromosome indicating the localization of the NHS gene on Xp22.13. Schematic organization of the NHS gene, exons in scale and three different molecular diagnostic techniques are shown. P1: Electropherogram of the NHS gene exon 6. P2: SNP array analysis. P3 and P4: WES analysisBack to article page