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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...
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| Fformat: | Artigo |
| Iaith: | Inglês |
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BioMed Central
2010
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| Mynediad Ar-lein: | 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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