Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

The identification of multilocus imprinting disturbances (MLID) appears fundamental to uncover molecular pathways underlying imprinting disorders (IDs) and to complete clinical diagnosis of patients. However, MLID genetic associated mechanisms remain largely unknown. To characterize MLID in Beckwith...

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Detalles Bibliográficos
Autores principales: Fontana, L., Bedeschi, M. F., Maitz, S., Cereda, A., Faré, C., Motta, S., Seresini, A., D’Ursi, P., Orro, A., Pecile, V., Calvello, M., Selicorni, A., Lalatta, F., Milani, D., Sirchia, S. M., Miozzo, M., Tabano, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284780/
https://www.ncbi.nlm.nih.gov/pubmed/30221575
http://dx.doi.org/10.1080/15592294.2018.1514230

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284780/
https://www.ncbi.nlm.nih.gov/pubmed/30221575
http://dx.doi.org/10.1080/15592294.2018.1514230

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