Prenatal ultrasonography and genetic analysis of fetal cleidocranial dysplasia: A case report

doi:10.12998/wjcc.v13.i10.97584

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 13, Issue 10

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 (799)

All Articles published online

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

Item

Count

PDF

HTML

265

Figures (1-3)

Tables (1-1)

Sum=460

Featured Article

The chart showing Browse series, Download series.

Item

Count

Browse

104

Download

145

Sum=249

Publishing Process of This Article

Item

Count

Browse

Download

Sum=68

Apr 6, 2025 (publication date) through Feb 21, 2025

Times Cited of This Article

Times Cited (0)

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. Apr 6, 2025; 13(10): 97584
Published online Apr 6, 2025. doi: 10.12998/wjcc.v13.i10.97584

Full Size Figure Download Figure

Figure 2 Sequencing results show that the fetus carried pathogenic mutations in the RUNX2 gene (c. 674G>A) (black arrow).

Citation: Wang F, Dai PF, Gao WJ. Prenatal ultrasonography and genetic analysis of fetal cleidocranial dysplasia: A case report. World J Clin Cases 2025; 13(10): 97584
URL: https://www.wjgnet.com/2307-8960/full/v13/i10/97584.htm
DOI: https://dx.doi.org/10.12998/wjcc.v13.i10.97584