Three novel FOXL2 gene mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
- Author:
Siu-fong June OR
1
;
Ming-for Tony TONG
;
Fai-man Ivan LO
;
Tak-sum Stephen LAM
Author Information
1. Clinical Genetic Service, Department of Health, Hong Kong SAR, China.
- Publication Type:Journal Article
- MeSH:
Abnormalities, Multiple;
genetics;
Amino Acid Sequence;
Blepharophimosis;
genetics;
Blepharoptosis;
genetics;
Eyelids;
abnormalities;
Female;
Forkhead Box Protein L2;
Forkhead Transcription Factors;
genetics;
Humans;
Male;
Molecular Sequence Data;
Mutation;
Syndrome
- From:
Chinese Medical Journal
2006;119(1):49-52
- CountryChina
- Language:English
