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Epigenetics in Turner syndrome
BACKGROUND: Monosomy of the X chromosome is the most frequent genetic abnormality in human as it is present in approximately 2% of all conceptions, although 99% of these embryos are spontaneously miscarried. In postnatal life, clinical features of Turner syndrome may include typical dysmorphic stigm...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889574/ https://www.ncbi.nlm.nih.gov/pubmed/29636833 http://dx.doi.org/10.1186/s13148-018-0477-0 |