A review of trisomy X (47,XXX)

Trisomy X is a sex chromosome anomaly with a variable phenotype caused by the presence of an extra X chromosome in females (47,XXX instead of 46,XX). It is the most common female chromosomal abnormality, occurring in approximately 1 in 1,000 female births. As some individuals are only mildly affecte...

Descripción completa

Detalles Bibliográficos
Autores principales: Tartaglia, Nicole R, Howell, Susan, Sutherland, Ashley, Wilson, Rebecca, Wilson, Lennie
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883963/
https://www.ncbi.nlm.nih.gov/pubmed/20459843
http://dx.doi.org/10.1186/1750-1172-5-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883963/
https://www.ncbi.nlm.nih.gov/pubmed/20459843
http://dx.doi.org/10.1186/1750-1172-5-8

Ejemplares similares