Figure 1From: Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case reportFamily pedigree showing the haplotypes and analytical findings. In addition to the c.418 G>A mutation, the genotypes for the intron 3+c.123 C>T, exon 8 c.942 T>C, and intron 12+c.267 G>C are also indicated.Back to article page