Frequency of WT1 and 11p15 constitutional aberrations and phenotypic correlation in childhood Wilms tumour patients

Keyphrases

• Aberrations 100%
• Wilms Tumor 100%
• Tumor Patients 100%
• Phenotypic Correlation 100%
• Beckwith-Wiedemann Syndrome 37%
• Molecular Analysis 25%
• Clinical Genetics 25%
• Phenotypic Abnormalities 25%
• Genetic Counseling 12%
• Histology 12%
• Genetic Predisposition 12%
• Bilateral Disease 12%
• Aniridia 12%
• WAGR Syndrome 12%
• Genitourinary Anomalies 12%
• Chromosome 11p15 12%
• Epigenetic Modification 12%
• WT1 mutation 12%
• Single Center 12%
• Intellectual Disability 12%
• Young Age 12%
• Congenital Anomalies 12%
• Overgrowth Syndrome 12%
• Genetic Evaluation 12%
• Syndromic 12%
• Clinical Signs 12%
• Clinical Assessment 12%
• Genitourinary Malformations 12%
• Patient Analysis 12%
• Assessment Analysis 12%
• Associated Syndromes 12%
• Denys-Drash Syndrome 12%
• Hemihypertrophy 12%

Biochemistry, Genetics and Molecular Biology

• Wilms' Tumor 100%
• WT1 100%
• Beckwith-Wiedemann Syndrome 37%
• Genetics 12%
• Genetic Predisposition 12%
• Genetic Counseling 12%
• Epigenetics 12%
• WAGR Syndrome 12%
• Aniridia 12%

Medicine and Dentistry

• Wilms' Tumor 100%
• Beckwith Wiedemann Syndrome 37%
• Clinical Genetics 25%
• Disease 12%
• Genetic Counseling 12%
• Genetic Predisposition 12%
• Aniridia 12%
• WAGR Syndrome 12%
• Congenital Malformation 12%
• Clinical Assessment 12%
• Urogenital Tract Malformation 12%
• Hemihypertrophy 12%
• Denys Drash Syndrome 12%