Cytogenetic and genomic analysis of a patient with turner syndrome and t(2;12): a case report

BACKGROUND: Turner syndrome is a genetic disorder that affects women. It is caused by an absent or incomplete X chromosome, which can be presented in mosaicism or not. There are 12 cases of Turner syndrome patients who present structural alterations in autosomal chromosomes. CASE PRESENTATION: The p...

Descripción completa

Detalles Bibliográficos
Autores principales: Leone, Paola E., Yumiceba, Verónica, Jijón-Vergara, Ariana, Pérez-Villa, Andy, Armendáriz-Castillo, Isaac, García-Cárdenas, Jennyfer M., Guerrero, Santiago, Guevara-Ramírez, Patricia, López-Cortés, Andrés, Zambrano, Ana K., Hernández-Rivas, Jesús M., García, Juan Luis, Paz-y-Miño, César
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664101/
https://www.ncbi.nlm.nih.gov/pubmed/33292387
http://dx.doi.org/10.1186/s13039-020-00515-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664101/
https://www.ncbi.nlm.nih.gov/pubmed/33292387
http://dx.doi.org/10.1186/s13039-020-00515-0

Ejemplares similares