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Chromosomal rearrangement interferes with meiotic X chromosome inactivation
Heterozygosity for certain mouse and human chromosomal rearrangements is characterized by the incomplete meiotic synapsis of rearranged chromosomes, by their colocalization with the XY body in primary spermatocytes, and by male-limited sterility. Previously, we argued that such X–autosomal associati...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Cold Spring Harbor Laboratory Press
2007
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1987340/ https://ncbi.nlm.nih.gov/pubmed/17717048 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.6520107 |
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