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Figure 1 | Journal of Medical Case Reports

Figure 1

From: Triple X syndrome in a patient with partial lipodystrophy discovered using a high-density oligonucleotide microarray: a case report

Figure 1

X chromosome probe intensity for copy number determination. Copy number determination was performed using 130 normal controls (65 men, 65 women) and 40 lipodystrophy cases (29 women, 11 men). Red dots represent single nucleotide polymorphism intensity for 29 female lipodystrophy patients. Green dots represent SNP intensity for 11 male lipodystrophy patients. Blue dots represent single nucleotide polymorphism intensity for the female lipodystrophy patient diagnosed with triple X syndrome. For the patient with triple X syndrome, probe intensities were within the normal range for all other chromosomes, with the exception of the duplication on 5q33.2 (data not shown).

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