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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Tartaglia, Nicole R, Howell, Susan, Sutherland, Ashley, Wilson, Rebecca, Wilson, Lennie
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2010
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2883963/
https://ncbi.nlm.nih.gov/pubmed/20459843
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-5-8
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