1.
Ann Genet
; 33(1): 56-9, 1990.
Artigo
em Inglês
| MEDLINE
| ID: mdl-2195984
RESUMO
Two half-sisters with distal monosomy of the long arm of chromosome 6 (q25----qter) inherited by maternal translocation t(6q;17q) were investigated. The clinical manifestations of these patients are compared with eight cases reported in the literature for further characterization of the 6q-syndrome. The cytogenetic diagnosis of alterations involving small chromosome fragments and the different origins of this type of deletion are also discussed.