Skip to main content
Fig. 1 | BMC Medical Genomics

Fig. 1

From: X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene

Fig. 1

Pedigrees of the 3 Families (F1, F2, and F3): Haplotype study was performed in the 8 patients and in three of their mothers. Genotyping results for 7 microsatellites markers DXS1060, DXS8105, DXS996, DXS1223, DXS8051, DXS7103, and DXS7108 are shown. No common haplotype was shared by the three families. (The numbers in the male and female symbols in family 3 correspond to the number of siblings in the same generation. The red arrows correspond to patients who have undergone CGH array testing)

Back to article page

BMC Medical Genomics

ISSN: 1755-8794

Contact us