Fig. 3From: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genesKaryotype of index-patient (III.1). Karyotyping (GTG-banding) of lymphocytes of peripheral blood revealed an inversion in the short arm of chromosome 1. Breakpoints in 1p31.3 and 1p36.31 (arrows) correspond to two deletions, which have been revealed by SNP array and depicted in Fig. 4 Back to article page