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Array-CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation

  • Published:2010-07-15 Issue:8 Volume:152A Page:2130-2133
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am. J. Med. Genet.

Author:

Gimelli Stefania,Divizia Maria Teresa,Lerone Margherita,Bricco Lara,Béna Frédérique,Antonarakis Stylianos E.,Ravazzolo Roberto,Gimelli Giorgio

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference10 articles.

Cited by 4 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. Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review;Molecular Syndromology;2022-02-11

2. Guidelines for genetic study of aniridia;Archivos de la Sociedad Española de Oftalmología (English Edition);2013-04

3. Guía para el estudio genético de la aniridia;Archivos de la Sociedad Española de Oftalmología;2013-04

4. Deletion and duplication of 11p13-11p14: Reciprocal aberrations derived from a paternal insertion;American Journal of Medical Genetics Part A;2011-09-19
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