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Figure 3 | Orphanet Journal of Rare Diseases

Figure 3

From: Anderson's disease/chylomicron retention disease in a Japanese patient with uniparental disomy 7 and a normal SAR1B gene protein coding sequence

Figure 3

Maternal uniparental disomy of chromosome 7 (matUPD7). An ideogram of chromosome 7 is shown surrounded, on the right, by a portion of the genotypes of the patient and his father and mother obtained by SNP analysis and the regions of isodisomy and heterodisomy that are inferred from the analysis. On the left, regions of complete homozygosity and regions containing both homozygosity and heterozygosity as determined by SNP analysis are shown. Red boxes show regions of non-Mendelian inheritance.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172