A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability
Figure 3
FISH study in the patient and her father. In each of them, 30 metaphases from cultured peripheral blood lymphocytes were analysed. (a) Patient metaphase showing one normal chromosome 14 [RP11-123M6 (green)/14 qter 9 (red)] and the del(14)(q32.2q32.31) with only 14 qter signal (red). (b) Metaphase from the father with a normal FISH pattern, indicating two normal chromosomes 14.
