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. 2005 Apr 29;90(8):807–812. doi: 10.1136/adc.2004.050799

Figure 5.

Figure 5

 SH/H data of the members of a family, with an HCH mutation in the FGFR3 gene on the maternal side, that caused a mild hypochondroplasia with a variable expression pattern. (A) SH/H index for the index case, her cousin, her mother, her aunt, and grandmother. (B) SH/H index for the brother and an uncle of the index case.