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

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.37.5.377
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

NOVEL Intronic CAPN3 Roma Mutation Alters Splicing Causing RNA Mediated Decay

Annals of Clinical and Translational Neurology
NeuroscienceNeurology
2019English

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

Oncogene
Cancer ResearchGeneticsMolecular Biology
2002English

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

Familial Cancer
Cancer ResearchOncologyGenetics
2010English

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

European Journal of Human Genetics
Genetics
2013English

Hypoglycaemia With Wilms' Tumour

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
1964English

Embryonal Precursors of Wilms Tumour

Nature Reviews Urology
Urology
2019English

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

Genes and Development
GeneticsDevelopmental Biology
1994English

Follow-Up Surveillance of Wilms' Tumour

The Lancet Oncology
Oncology
2018English

Wilm's Tumor-1 (WT1) Rs16754 Polymorphism

Turkish Journal of Haematology
Hematology
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy