Work

Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome

Year: 2010

Type: article

Study design: Case Report

Source: Journal of Human Genetics

DOI: 10.1038/jhg.2010.121

Authors: Hsiao-Mei Liao, Dau-Ming Niu, Yan-Jang Chen, Jye-Siung Fang, Shih-Jen Chen, Chia-Hsiang Chen

Institutions: National Tsing Hua University, Taipei Veterans General Hospital, National Yang Ming University, Taipei Municipal YangMing Hospital, Taipei City Hospital, Tzu Chi University, National Health Research Institutes, Chang Gung University, Linkou Chang Gung Memorial Hospital

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

Funder: National Health Research Institutes

OpenAlex ID: W1964237362

FWCI: 0.278

Cites: 18

Cited by: 31

Related to: 10