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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...

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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

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