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Figure 3 | BMC Medical Genetics

Figure 3

From: Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences

Figure 3

Phenotypic categories (A, B, C, D) in the affected subjects of the Pakistani (P) and Indian families (I). SPD1 phenotypic variants observed in the Pakistani and Indian family subjects, are grouped into four distinct clinical categories (A, B, C, D), drawn according to the scheme described by Malik et al. [8]. Genotypes for the GCN-region of HOXD13 are also provided (see Figures 1; 4).

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BMC Medical Genetics

ISSN: 1471-2350

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