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Publications by K. PRITCHARD-JONES

Familial Wilms Tumour Resulting From WT1 Mutation: Intronic Polymorphism Causing Artefactual Constitutional Homozygosity

Journal of Medical Genetics

English

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NOVEL Intronic CAPN3 Roma Mutation Alters Splicing Causing RNA Mediated Decay

Annals of Clinical and Translational Neurology

English

Changes in WT1 Splicing Are Associated With a Specific Gene Expression Profile in Wilms' Tumour

Cancer Research

Molecular Biology

English

An Intronic Mutation in MLH1 Associated With Familial Colon and Breast Cancer

Familial Cancer

Cancer Research

English

In Vitro Antisense Therapeutics for a Deep Intronic Mutation Causing Neurofibromatosis Type 2

European Journal of Human Genetics

English

Hypoglycaemia With Wilms' Tumour

Archives of Disease in Childhood

English

Embryonal Precursors of Wilms Tumour

Nature Reviews Urology

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RNA Editing in the Wilms' Tumor Susceptibility Gene, WT1.

Genes and Development

Developmental Biology

English

Follow-Up Surveillance of Wilms' Tumour

The Lancet Oncology

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Wilm's Tumor-1 (WT1) Rs16754 Polymorphism

Turkish Journal of Haematology

English