A submicroscopic deletion of 11p13 associated with the WAGR syndrome-Reference-Cited by-同舟云学术

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A submicroscopic deletion of 11p13 associated with the WAGR syndrome

Published:2003-04 Issue:4 Volume:63 Page:319-322
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Nanclares Guiomar Pérez de,Martínez Francisco,Bilbao Jose Ramon,Navajas Aurora,Martínez Ricardo,López-Arístegui Ma Asunción,Castaño Luis

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2003.00051.x/fullpdf

Reference11 articles.

1. Association of Wilms' tumor with aniridia, hemihypertrophy and other congenital malformations;Miller;N Engl J Med,1964

2. Chromosomal imbalance in the aniridia-Wilms' tumor association: 11p interstitial deletion;Riccardi;Pediatrics,1978

3. Aniridia, cataract and gonadoblastoma in a mentally retarded girl with deletion of chromosome 11: a clinicopathological case report;Anderson;Ophthalmologica,1978

4. Chromosomal deletions and enzyme deficiencies;Schmickel;J Pediatr,1986

5. A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus;Crolla;J Med Genet,1997

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Vesicoureteric reflux and renal malformations: a developmental problem;Clinical Genetics;2006-01-04

2. WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH;American Journal of Medical Genetics Part A;2006

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