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Figure 2 | Molecular Cytogenetics

Figure 2

From: Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability

Figure 2

Analysis of family N. ( A ) The CNTN6 deletion in patient N. ( B ) Real-time PCR analysis of CNTN6: C1 - female control, C2 - male control, II-1 - patient N, I-1 - mother, I-2 - father; CNTN6_E22a and CNTN6_E22b - probes for exon 22, CNTN6_E23 - probe for exon 23. ( C ) The pedigree plot for family N; the dark, solid circle represents the affected patient N, and the gray, solid square represents father N.

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