Research Article
Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome
Figure 3
Large STK11 gene mutations detected by multiplex ligation-dependent probe amplification in patients with PJS. (a–c) The deletion of exon 1, exons 2-3, and exon 8, respectively.
(a) |
(b) |
(c) |