Achondroplasia in diverse Jewish and Arab populations in Israel: Clinical and molecular characterization

Keyphrases

• Achondroplasia 100%
• Arab Population 100%
• Arginine mutation 20%
• Atypical Forms 20%
• Autosomal Dominant 40%
• Clinical Characterization 100%
• Codon 60%
• De-novo mutations 20%
• Diverse Ethnic Groups 20%
• FGFR3 Gene 20%
• Fibroblast Growth Factor Receptor 3 (FGFR3) 20%
• Genetic Disease 20%
• Glycine 20%
• Israel 100%
• Jewish Patients 20%
• Jewish Population 100%
• Molecular Characterization 100%
• Rhizomelic Shortening 20%
• Short Stature 20%
• Sporadic Patient 20%
• Transmembrane Domain 20%

Biochemistry, Genetics and Molecular Biology

• Arginine 33%
• Autosomal Dominant Inheritance 66%
• Body Height 33%
• Codon 100%
• Dominant Inheritance 33%
• Fibroblast Growth Factor Receptor 3 33%
• Genetic Disorder 33%
• Transmembrane Domain 33%