1.
J Pediatr
; 145(6): 840-2, 2004 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15580214
RESUMO
We report a de novo cryptic 11p duplication found by genomic microarray with a cytogenetically detected 4p deletion. Terminal 4p deletions cause Wolf-Hirschhorn syndrome, but the phenotype probably was modified by the paternally derived 11p duplication. This emphasizes the clinical utility of genomic microarray.