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Blood, Vol. 112, Issue 13, 5238-5240, December 15, 2008 This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef Homozygous deletion of HFE produces a phenotype similar to the HFE p.C282Y/p.C282Y genotype Blood Le Gac et al. 112: 5238 Supplemental materials for: Le Gac et al Files in this Data Supplement: Table S1. Primer pairs used in the Mapping PCR and Gap PCR experiments (PDF, 11.9 KB) Figure S1. Semi-quantitative fluorescent multiplex PCR assay (JPG, 72 KB) - (A) The QFM-PCR electrophoregram of the reported case (lower panel) is compared to that of a control individual (upper panel). X-axis: size in bp; Y-axis: fluorescence intensity (arbitrary units). Exons under study are indicated at the top of the corresponding peaks. The control amplicon (CTL) was originated from an independent locus (located on chromosome 7). (B) The QFM-PCR electrophoregrams of a relative (red) and of a control individual (blue). Profiles were superimposed and then normalized using the control amplicon (CTL). Figure S2. Array-CGH of the reported case (JPG, 97.5 KB) - The vertical axis indicates chromosomal position in Mb, and the horizontal axis is the log2 ratio of the ratio of case channel to control channel. Grey box indicate positions and sizes of HFE and its neighbouring genes. This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef

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