Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report

doi:10.12998/wjcc.v11.i9.2036

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 11, Issue 9

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 (2474)

All Articles published online

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

Item

Count

PDF

143

WORD

HTML

1414

Figures (1-4)

342

Sum=1942

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

117

Download

405

Sum=522

Mar 26, 2023 (publication date) through Nov 22, 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. Mar 26, 2023; 11(9): 2036-2042
Published online Mar 26, 2023. doi: 10.12998/wjcc.v11.i9.2036

Full Size Figure Download Figure

Figure 1 Pedigree map of the family.

Citation: Shen R, Feng JH, Yang SP. Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report. World J Clin Cases 2023; 11(9): 2036-2042
URL: https://www.wjgnet.com/2307-8960/full/v11/i9/2036.htm
DOI: https://dx.doi.org/10.12998/wjcc.v11.i9.2036