A novelWT1mutation in familial wilms tumor-Reference-Cited by-同舟云学术

A novelWT1mutation in familial wilms tumor

Published:2013-03-28 Issue:8 Volume:60 Page:1388-1389
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Melchionda Fraia¹,Spreafico Filippo²,Ciceri Sara³,Lima Mario⁴,Collini Paola⁵,Pession Andrea¹,Massimino Maura²,Radice Paolo³,Perotti Daniela³

Affiliation:

1. Pediatric Oncology and Hematology Unit “Lalla Seràgnoli”, Department of Pediatrics; University of Bologna Sant'Orsola-Malpighi Hospital; Bologna; Italy

2. Pediatric Oncology Unit, Department of Hematology and Pediatric Hemato-Oncology; Fondazione IRCCS Istituto Nazionale dei Tumori; Milan; Italy

3. Molecular Bases of Genetic Risk and Genetic Testing Unit, Department of Preventive and Predictive Medicine; Fondazione IRCCS Istituto Nazionale dei Tumori; Milan; Italy

4. Pediatric Surgery Unit, Department of Pediatric Surgery; University of Bologna, Sant'Orsola-Malpighi Hospital; Bologna; Italy

5. Department of Pathology and Laboratory Medicine; Fondazione IRCCS Istituto Nazionale dei Tumori; Milan; Italy

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference6 articles.

1. Familial Wilms' tumor: A descriptive study;Breslow;Med Pediatr Oncol,1996

2. Familial occurrence of the Aniridia-Wilms tumor syndrome with deletion 11p13-14. 1;Yunis;J Pediatr,1980

3. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour;Pelletier;Nature,1991

4. Familial Wilms' tumor associated with a WT1 zinc finger mutation;Kaplinsky;Genomics,1996

5. Familial Wilms tumour resulting from WT1 mutation: intronic polymorphism causing artefactual constitutional homozygosity;Pritchard-Jones;J Med Genet,2000

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