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Fig. 2 | Molecular Cytogenetics

Fig. 2

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. 2

The genomic region deleted in the present patient (black horizontal bar) and in the previously reported cases (grey bars) [21, 2329, 33]. The Ms5Yah mouse model (horizontal striped bar) and the regions (Region 1–3, horizontal white bars) proposed by Lyle et al. [21] are also shown. The genes shown in the figure are UCSC genes (genes that have a corresponding entry in the Protein Data Bank or the transcript has been reviewed or validated by either the RefSeq, SwissProt or CCDS staff)

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