Work

Single‐Gene Deletion of FGF3 in a Patient With Features of 11q13 Microdeletion Syndrome

Year: 2025

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.64025

Authors: Hamed Rahi, Patricia I. Dickson, Tomi L. Toler, Meagan M. Corliss, Yang Cao

Institution: Washington University in St. Louis

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4407779554

FWCI:

Cites: 16

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Related to: 10