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Association between telomere length and chromosome 21 nondisjunction in the oocyte
Chromosome 21 nondisjunction in oocytes is the most common cause of trisomy 21, the primary chromosomal abnormality responsible for Down syndrome (DS). This specific type of error is estimated to account for over 90% of live births with DS, with maternal age being the best known risk factor for chro...
Tallennettuna:
| Julkaisussa: | Hum Genet |
|---|---|
| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4630140/ https://ncbi.nlm.nih.gov/pubmed/26407969 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-015-1603-0 |
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