en
Scientific article
Case report
English

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 inAmerican journal of medical genetics. Part A, vol. 152A, no. 8, p. 2130-2133
Publication date2010
Keywords
  • Chromosomes, Human, Pair 11/*genetics
  • Chromosomes, Human, Pair 2/*genetics
  • *Comparative Genomic Hybridization
  • Fathers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant, Newborn
  • Male
  • *Oligonucleotide Array Sequence Analysis
  • Translocation, Genetic/*genetics
  • WAGR Syndrome/*genetics
Citation (ISO format)
GIMELLI, Stefania et al. Array-CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation. In: American journal of medical genetics. Part A, 2010, vol. 152A, n° 8, p. 2130–2133. doi: 10.1002/ajmg.a.33517
Main files (1)
Article
accessLevelRestricted
Identifiers
ISSN of the journal1552-4825
464views
0downloads

Technical informations

Creation05/23/2012 8:45:40 AM
First validation05/23/2012 8:45:40 AM
Update time03/14/2023 5:33:15 PM
Status update03/14/2023 5:33:15 PM
Last indexation02/12/2024 8:12:56 PM
All rights reserved by Archive ouverte UNIGE and the University of GenevaunigeBlack