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Fig. 1 | Molecular Cytogenetics

Fig. 1

From: Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development

Fig. 1

Chromosomal microarray overview from chromosome 21 displaying the deletion at 21q11.2q22.11 (15218106-33265774)x1 (a); FISH signals on metaphase chromosomes of the patient using the 21qter probe. One of the signals is on the normal chromosome 21 (arrow head) and the other signal on the derivative chromosome 12 (arrow) (b); The clinical pictures of the patient at age 5 months (c) and at age 1 year (d)

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