Gene diagnosis of infantile neurofibromatosis type I: A case report

doi:10.12998/wjcc.v8.i22.5678

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 8, Issue 22

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 (6923)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-4) series.

Item

Count

PDF

187

WORD

148

HTML

5067

Figures (1-4)

300

Sum=5702

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

452

Download

769

Sum=1221

Nov 26, 2020 (publication date) through May 16, 2024

Times Cited of This Article

Times Cited (1)

Journal Information of This Article

Publication Name

World Journal of Clinical Cases

ISSN

2307-8960

Publisher of This Article

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

Case Report

World J Clin Cases. Nov 26, 2020; 8(22): 5678-5683
Published online Nov 26, 2020. doi: 10.12998/wjcc.v8.i22.5678

Full Size Figure Download Figure

Figure 3 Large areas of brown pigmentation were noted on the lower limbs, feet, buttocks, and perineum.

Citation: Li MZ, Yuan L, Zhuo ZQ. Gene diagnosis of infantile neurofibromatosis type I: A case report. World J Clin Cases 2020; 8(22): 5678-5683
URL: https://www.wjgnet.com/2307-8960/full/v8/i22/5678.htm
DOI: https://dx.doi.org/10.12998/wjcc.v8.i22.5678