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Fig. 4 | Molecular Cytogenetics

Fig. 4

From: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

Fig. 4

SNP Array on DNA from peripheral blood leukocytes. a Two deletions are revealed in the short arm of chromosome 1 in both the index-patient (III.1) and her mother (II.1). The distal deletion maps in band 1p36.31 and spans over 211 Kb (b) and the proximal deletion maps in band 1p31.3 and spans over 271 Kb (c). (GRC37h/hg19 genome build)

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