The genetic architecture of aniridia and Gillespie syndrome

Biochemistry, Genetics and Molecular Biology

• Aniridia 100%
• Genetic Architecture 100%
• PAX6 30%
• Mental Retardation 30%
• Regulatory Region 20%
• Genetics 20%
• Development 20%
• Nested Gene 20%
• Mutation 10%
• ACTA2 10%
• PITX2 10%
• Wilms' Tumor 10%
• WAGR Syndrome 10%
• Stop Codon 10%
• C-Terminus 10%
• Life 10%
• Phenotype 10%
• Light 10%
• Loss of Function Mutation 10%
• Allele 10%
• ITPR1 10%
• WT1 10%
• Molecular Genetics 10%
• Chromosome 11p 10%

Medicine and Dentistry

• Aniridia 100%
• Syndrome 100%
• Iris 40%
• Eye Malformation 20%
• Aplasia 10%
• Clinical Feature 10%
• Brain Derived Neurotrophic Factor 10%
• Obesity 10%
• WAGR Syndrome 10%
• Hypoplasia 10%
• Loss of Function Mutation 10%
• Carboxy Terminal Sequence 10%
• Sphincter 10%
• Wilms' Tumor 10%
• Cerebellar Ataxia 10%
• Prematurity 10%
• Stop Codon 10%
• Smooth Muscle 10%
• Congenital Malformation 10%
• Chromosome 11p 10%
• Absence 10%
• Phenotype 10%