Skip to main content
Figure 2 | BMC Medical Genetics

Figure 2

From: Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype

Figure 2

Array-CGH analysis showing a deletion of approximately 1.5 Mb that involved the 1p36.33 region, with the breakpoint falling between 554,268 bp and 2,133,973 bp (2a), and a deletion of approximately 2.5 Mb that involved the 1p36.33 – 1p36.32 region, with the breakpoint falling between 564,424 bp and 3,111,905 bp (2b).

Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us