Journal article

A clinical overview of WT1 gene mutations

M Little, C Wells

Human Mutation | WILEY | Published : 1997

DOI: 10.1002/(SICI)1098-1004(1997)9:3<209::AID-HUMU2>3.0.CO;2-2

University of Melbourne Researchers

Christine Wells Author Anatomy and Neuroscience

Melissa Little Author Paediatrics Royal Children's Hospital

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Keywords

Tumour Suppressor

Mental Retardation

Familial Predisposition

Wiedemann-Beckwith Syndrome

Wilms-Tumor Gene

Nephrotic Syndrome

Chromosome Deletion

Genes, Tumor Suppressor

Dominant-Negative Fashion

3rd Zinc-Finger

Suppressor Gene

Genetics & Heredity

Genes, Wilms Tumor

Denys-Drash Syndrome

Gene Expression Regulation, Neoplastic

Disorders of Sex Development

Urogenital Development

Point Mutations

Science & Technology

Kidney Neoplasms

Beckwith-Wiedemann Syndrome

Life Sciences & Biomedicine

Chromosomes, Human, Pair 11