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

Wiedemann-Beckwith Syndrome

Kidney Neoplasms

Genetics & Heredity

3rd Zinc-Finger

Suppressor Gene

Gene Expression Regulation, Neoplastic

Chromosome Deletion

Mental Retardation

Denys-Drash Syndrome

Point Mutations

Nephrotic Syndrome

Genes, Tumor Suppressor

Tumour Suppressor

Genes, Wilms Tumor

Urogenital Development

Life Sciences & Biomedicine

Dominant-Negative Fashion

Science & Technology

Disorders of Sex Development

Chromosomes, Human, Pair 11

Familial Predisposition

Wilms-Tumor Gene

Beckwith-Wiedemann Syndrome