Work

[FGFR2 gene mutation in a Chinese patient with Apert syndrome].

Year: 2010

Type: article

Study design: Case Report

Source: PubMed

DOI: 10.3760/cma.j.issn.1003-9406.2010.06.018

Authors: Li Dai, Na-na Li, Yu-mei Yuan, Yong Liu, Jun Zhu

Institutions: Sichuan University, West China Second University Hospital of Sichuan University

Language: Chinese

Topic: Craniofacial Disorders and Treatments

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2419291807

FWCI:

Cites:

Cited by: 1

Related to: 10