Genetics and variation in phenotype in Noonan syndrome.

Keyphrases

• Noonan Syndrome 100%
• PTPN11 Gene 40%
• Autosomal Dominant 20%
• Short Stature 20%
• Facial Features 20%
• Familial Cases 20%
• Exon 4 20%
• Mutation Analysis 20%
• Congenital Heart Defects 20%
• Nijmegen 20%
• PTPN11 20%
• Exon 3 20%
• Exon 8 20%
• Juvenile Myelomonocytic Leukemia 20%
• Multiple Congenital Anomalies 20%
• SH2 Domain 20%
• SHP2 20%
• Clinical Entities 20%
• Receptor Protein Tyrosine Phosphatase 20%

Biochemistry, Genetics and Molecular Biology

• Genetics 100%
• Exon 100%
• PTPN11 100%
• Autosomal Dominant Inheritance 33%
• Body Height 33%
• Protein Tyrosine Phosphatase 33%
• SH2 Domain 33%