Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report

doi:10.12998/wjcc.v8.i24.6465

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 8, Issue 24

This Article

Academic Content and Language Evaluation of This Article

CrossCheck and Google Search of This Article

Academic Rules and Norms of This Article

Supplementary Materials 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 (5575)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-3) series.

Item

Count

PDF

235

WORD

184

HTML

3039

Figures (1-3)

272

Sum=3730

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

486

Download

1359

Sum=1845

Dec 26, 2020 (publication date) through Nov 5, 2024

Times Cited of This Article

Times Cited (3)

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. Dec 26, 2020; 8(24): 6465-6472
Published online Dec 26, 2020. doi: 10.12998/wjcc.v8.i24.6465

Full Size Figure Download Figure

Figure 1 Pictures of our patient at age 3 years. A-C: Facial characteristics; D: Dental abnormalities; E and F: Hands.

Citation: Li JR, Huang Z, Lu Y, Ji QY, Jiang MY, Yang F. Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report. World J Clin Cases 2020; 8(24): 6465-6472
URL: https://www.wjgnet.com/2307-8960/full/v8/i24/6465.htm
DOI: https://dx.doi.org/10.12998/wjcc.v8.i24.6465