Clinical features, endoscopic polypectomy and STK11 gene mutation in a nine-month-old Peutz-Jeghers syndrome Chinese infant

doi:10.3748/wjg.v22.i11.3261

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 22, Issue 11

This Article

Academic Content and Language Evaluation of This Article

CrossCheck and Google Search of This Article

Academic Rules and Norms of This Article

Citation of this article

Corresponding Author of This Article

Research Domain of This Article

Article-Type of This Article

Open-Access Policy of This Article

Times Cited Counts in Google of This Article

Number of Hits and Downloads for This Article

Total Article Views (7711)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-5) series, Tables (1-1) series.

Item

Count

PDF

519

WORD

232

HTML

3512

Figures (1-5)

198

Tables (1-1)

189

Sum=4650

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

1053

Download

2008

Sum=3061

Mar 21, 2016 (publication date) through Jul 17, 2024

Times Cited of This Article

Times Cited (6)

Journal Information of This Article

Publication Name

World Journal of Gastroenterology

ISSN

1007-9327

Publisher of This Article

Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Observational Study

World J Gastroenterol. Mar 21, 2016; 22(11): 3261-3267
Published online Mar 21, 2016. doi: 10.3748/wjg.v22.i11.3261

Full Size Figure Download Figure

Figure 5 Infant had a frameshift mutation in codon 64 (64_65het_delAT) in exon 1. The arrow indicates the mutation site.

Citation: Huang ZH, Song Z, Zhang P, Wu J, Huang Y. Clinical features, endoscopic polypectomy and STK11 gene mutation in a nine-month-old Peutz-Jeghers syndrome Chinese infant. World J Gastroenterol 2016; 22(11): 3261-3267
URL: https://www.wjgnet.com/1007-9327/full/v22/i11/3261.htm
DOI: https://dx.doi.org/10.3748/wjg.v22.i11.3261