[[abstract]]Objectives: The fibroblast growth factor receptor 3 gene (FGFR3) plays a critical role in cartilage growth-plate differentiation and bony development. It has been shown that 97% of patients with achondroplasia have a G to A transition mutation at position 1138 (c.1138 G>A) of codon 380 of the FGFR3 gene. Design and methods: Exon 8 of the FGFR3 gene was analyzed in 40 patients with achondroplasia, as well as in 50 control individuals for the presence of the c.1138G>A variant using melting curve analysis with a high-resolution melting instrument (HR-1). Results: The high-resolution melting curve analysis successfully genotyped the c.1138G>A mutation in exon 8 of the FGFR3 gene in all 40 patients with achondroplasia without the nee...
Background. Achondroplasia (ACH) represents the major cause of dwarfi sm and is due to mutations in ...
Mutations in the gene for fibroblast growth factor receptor 3 (FGFR3) are implicated in achondroplas...
L'achondroplasie est une maladie génétique rare représentant la forme la plus courante de nanisme à ...
Objectives: The fibroblast growth factor receptor 3 gene ( FGFR3) plays a critical role in cartilage...
Introduction: Achondroplasia (ACH) is the most common form of skeletal dysplasia of genetic origin i...
Achondroplasia is the most common genetic form of dwarfism inherited as an autosomal dominant disord...
Achondroplasia is the most common genetic form of dwarfism inherited as an autosomal dominant disord...
Achondroplasia is the most common genetic form of dwarfism inherited as an autosomal dominant disord...
Achondroplasia is the most common genetic form of dwarfism inherited as an autosomal dominant disord...
Achondroplasia and hypochondroplasia are common types of dwarfism in the Chinese population (Hwu ...
Achondroplasia, the most common form of short-limbed dwarfism in humans, occurs between 1 in 15,000 ...
Missense mutations in the tyrosine kinase receptor FGFR3 (Fibroblast Growth Factor Receptor 3) lead ...
Missense mutations in the tyrosine kinase receptor FGFR3 (Fibroblast Growth Factor Receptor 3) lead ...
Achondroplasia is an autosomal dominant disorder of rhizomelic dwarfism. It is predominantly caused ...
Achondroplasia is an autosomal dominant disorder of rhizomelic dwarfism. It is predominantly caused ...
Background. Achondroplasia (ACH) represents the major cause of dwarfi sm and is due to mutations in ...
Mutations in the gene for fibroblast growth factor receptor 3 (FGFR3) are implicated in achondroplas...
L'achondroplasie est une maladie génétique rare représentant la forme la plus courante de nanisme à ...
Objectives: The fibroblast growth factor receptor 3 gene ( FGFR3) plays a critical role in cartilage...
Introduction: Achondroplasia (ACH) is the most common form of skeletal dysplasia of genetic origin i...
Achondroplasia is the most common genetic form of dwarfism inherited as an autosomal dominant disord...
Achondroplasia is the most common genetic form of dwarfism inherited as an autosomal dominant disord...
Achondroplasia is the most common genetic form of dwarfism inherited as an autosomal dominant disord...
Achondroplasia is the most common genetic form of dwarfism inherited as an autosomal dominant disord...
Achondroplasia and hypochondroplasia are common types of dwarfism in the Chinese population (Hwu ...
Achondroplasia, the most common form of short-limbed dwarfism in humans, occurs between 1 in 15,000 ...
Missense mutations in the tyrosine kinase receptor FGFR3 (Fibroblast Growth Factor Receptor 3) lead ...
Missense mutations in the tyrosine kinase receptor FGFR3 (Fibroblast Growth Factor Receptor 3) lead ...
Achondroplasia is an autosomal dominant disorder of rhizomelic dwarfism. It is predominantly caused ...
Achondroplasia is an autosomal dominant disorder of rhizomelic dwarfism. It is predominantly caused ...
Background. Achondroplasia (ACH) represents the major cause of dwarfi sm and is due to mutations in ...
Mutations in the gene for fibroblast growth factor receptor 3 (FGFR3) are implicated in achondroplas...
L'achondroplasie est une maladie génétique rare représentant la forme la plus courante de nanisme à ...