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Figure 1 | BMC Medical Genetics

Figure 1

From: Novel mutations in natriuretic peptide receptor-2 gene underlie acromesomelic dysplasia, type maroteaux

Figure 1

Pedigrees of six consanguineous Pakistani families segregating autosomal recessive form of AMDM. Double lines are indicative of consanguineous union. Clear symbols represent unaffected individuals while filled symbols represent affected individuals. The diagonal line through a symbol is indicative of a deceased family member. Symbols with asterisks indicate individuals who were clinically examined and for whom DNA samples were available for molecular analysis.

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