1.
Clin Dysmorphol
; 15(4): 221-223, 2006 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16957477
RESUMO
We report a mother and son with an interstitial deletion of chromosome 2: del(2)(p21p22.2). Both have mildly dysmorphic facial features and learning difficulties. This phenotype contrasts with two previously described cases with a similar deletion that presented with cyclopia and alobar holoprosencephaly.