Trisomy in humans: incidence, origin and etiology.
Curr Opin Genet Dev
; 3(3): 398-403, 1993 Jun.
Article
em En
| MEDLINE
| ID: mdl-8353412
ABSTRACT
Molecular studies conducted over the past year have demonstrated the importance of aberrant genetic recombination in the etiology of several human trisomies, and have begun to shed light on the basis of the association between advancing maternal age and trisomy. Preliminary studies of gametes using fluorescence in situ hybridization indicate that this will be a useful approach in the analysis of human non-disjunction.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Trissomia
Tipo de estudo:
Etiology_studies
/
Incidence_studies
/
Prognostic_studies
/
Risk_factors_studies
Limite:
Animals
/
Humans
Idioma:
En
Revista:
Curr Opin Genet Dev
Assunto da revista:
GENETICA
Ano de publicação:
1993
Tipo de documento:
Article