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
Identifiers
- PID : unige:20966
- DOI : 10.1002/ajmg.a.33517
- PMID : 20635368
ISSN of the journal1552-4825
