Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference36 articles.
1. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
2. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
3. Common mutations in the fibroblast growth factor receptor 3 (FGFR3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism
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