An improved tetra-primer PCR approach for the detection of the FGFR3 G380R mutation responsible for achondroplasia
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology
Reference12 articles.
1. Mutations in the trans-membrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia;Shiang;Cell,1994
2. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia;Rousseau;Nature,1994
3. Achondroplasia is defined by recurrent G380R mutations of FGFR3;Bellus;Am J Hum Genet,1995
4. An improved methodology for the detection of the common mutation in the FGFR3 gene responsible for achondroplasia;Lanning;Hum Mutat,1997
5. Accurate diagnosis of a homozygous G1138A mutation in the fibroblast growth factor receptor 3 gene responsible for achondroplasia;Satiroglu-Tufan;Tohoku J Exp Med,2006
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