Mutation analysis of Crouzon syndrome in Taiwanese patients-Reference-Cited by-同舟云学术

Mutation analysis of Crouzon syndrome in Taiwanese patients

Published:2006-01 Issue:1 Volume:20 Page:23-26
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J. Clin. Lab. Anal.

Author:

Chang Chin‐Ping¹²,Wan Lei¹²³,Tsai Chang‐Hai³,Lee Cheng‐Chun¹,Tsai Fuu‐Jen¹⁴²⁵

Affiliation:

1. Department of Medical Research, China Medical University Hospital, Taichung, Taiwan

2. Department of Medical Genetics, China Medical University Hospital, Taichung, Taiwan

3. Asia University, Taichung, Taiwan

4. Department of Pediatrics, China Medical University Hospital, Taichung, Taiwan

5. College of Chinese Medicine, China Medical University, Taichung, Taiwan

Funder

China Medical University Hospital

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry, medical,Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.20096

Reference18 articles.

1. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

2. Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability

3. Predisposition for cysteine substitutions in the immunoglobulin-like chain of FGFR2 in Crouzon syndrome

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3. Genetics of Craniosynostosis;Youmans Neurological Surgery;2011

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