Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome

Figure 2

Variant spectrum of the STK11 gene detected in our study. (a) Schematic of the localization of 22 STK11 mutations; the numbers in parentheses indicate that the variation existed in several unrelated families. (b) Chromatogram of 8 novel STK11 gene mutations; mutations are indicated by arrows.

(a)

(b)