1.
Cancer Genet Cytogenet
; 63(1): 76-7, 1992 Oct 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-1423232
2.
Cancer Genet Cytogenet
; 55(1): 133-4, 1991 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-1913601
3.
Ann Genet
; 37(4): 196-9, 1994.
Artigo
em Inglês
| MEDLINE
| ID: mdl-7710255
RESUMO
The authors report the case of a girl with psychomotor and growth retardation, ventricular septal defect, patent ductus arteriosus, bulging forehead, prominent philtrum, low nasal bridge, inner epicanthal folds, strabismus, miosis, low set ears with prominence of antihelices, short neck, single transverse crease and camptodactyly of the fourth finger in both hands. G-banded chromosomal analysis revealed a 46, XX, del (6) (p23) chromosome constitution. A review of the phenotypes of the patients known with this chromosome deletion is presented.