Latest papers

WAGR syndrome with deletion of chromosome 11p11.2-13.

Focal segmental glomerulosclerosis in solitary kidney in WAGR syndrome.

Characteristics and outcomes of children with the Wilms tumor-Aniridia syndrome: a report from the National Wilms Tumor Study Group.

Cloning, functional study and comparative mapping of Luzp2 to mouse chromosome 7 and human chromosome 11p13-11p14.

A submicroscopic deletion of 11p13 associated with the WAGR syndrome.

Missense mutations in the DNA-binding region and termination codon in PAX6.

Recent advances in Wilms tumor genetics.

Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadias.

Morbid obesity and hyperphagia in the WAGR syndrome.

Clinical and molecular evidence for the role of androgens and WT1 in testis descent.

A case of atypical WAGR syndrome with anterior segment anomaly and microphthalmos.

Anaesthetic management for a patient with WAGR syndrome.

WAGR syndrome in a baby--the result of 6-MP treatment in a father affected by Crohn's disease?

Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromes.

Obesity and WAGR syndrome.

Detailed transcript map of a 810-kb region at 11p14 involving identification of 10 novel human 3' exons.

[WAGR syndrome: a case report]

The 239AB gene on chromosome 22: a novel member of an ancient gene family.

A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.

A clinical overview of WT1 gene mutations.