Lataa...
Microdeletions in FMR2 may be a significant cause of premature ovarian failure
Genetic causes of premature ovarian failure (POF) include X chromosome deletions and fragile X (FRAXA) premutations. While screening a cohort of women with POF for FRAXA premutations, a more distal trinucleotide repeat, FRAXE, was also tested. We found an unexpected excess of FRAXE alleles with appa...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Group
1999
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1734234/ https://ncbi.nlm.nih.gov/pubmed/10528856 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|