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. 2017 Jul 14;1(8):1104–1109. doi: 10.1210/js.2017-00164

Figure 2.

Figure 2.

Sequencing electropherogram of NSD1 exon 23 from the patient (top) and her parents (bottom). The double peak (in blue) confirms the presence of a de novo heterozygous missense mutation at c.6605G>C (p.Cys2202Ser). No mutation was found in the patient's mother and father.