1.
J Med Genet
; 26(3): 205-6, 1989 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-2468775
2.
Ann Genet
; 31(4): 247-9, 1988.
Artigo
em Inglês
| MEDLINE
| ID: mdl-3265310
RESUMO
A new case of monosomy 21 was observed in a newborn male. Characteristic clinical features include: an antimongoloid eye slants, large and low set ears, flat nose bridge, hypoplastic nipples, cardiac anomalies, muscular hypotonia, retarded psychomotor development. The karyotypes of the parents were normal.
