X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes
Kaydedildi:
| Yazarlar: | , , , |
|---|---|
| Materyal Türü: | artículo original |
| Yayın Tarihi: | 1995 |
| Diğer Bilgiler: | Artículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 1995. Este documento es privado debido a limitaciones de derechos de autor. |
| Ülke: | Kérwá |
| Kurum: | Universidad de Costa Rica |
| Repositorio: | Kérwá |
| OAI Identifier: | oai:kerwa.ucr.ac.cr:10669/15073 |
| Online Erişim: | http://link.springer.com/article/10.1007%2FBF00207374 https://hdl.handle.net/10669/15073 |
| Anahtar Kelime: | Duchenne muscular dystrophy polimorfismo genético Genética humana |