Journal of Human Genetics

FIGURE 3

FROM:

Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis

Shozo Honda, Shin Hayashi, Issei Imoto, Jun Toyama, Hitoshi Okazawa, Eiji Nakagawa, Yu-ichi Goto and Johji Inazawa, Japanese Mental Retardation Consortium

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Figure 3.

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Pedigrees of 10 families in which probable pCNVs were detected. Closed squares and circles, gray squares and circles, and dotted circles indicate MR, borderline MR and carrier, respectively. The proband indicated by an arrow was used for CGH with the X-tiling array. Asterisks indicate persons having identical pCNVs among each family. A slash indicates that the person has died. NA, not available.

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