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

Gimelli, Stefania

Array-CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation. [electronic resource] - American journal of medical genetics. Part A Aug 2010 - 2130-3 p. digital

Publication Type: Case Reports; Journal Article

1552-4833

10.1002/ajmg.a.33517 doi


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