Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X

Turner Syndrome is characterized by a normal X chromosome and the partial or complete absence of a second sexual chromosome. Small supernumerary marker chromosomes are present in 6.6% of these patients. Because of the wide range of Turner syndrome karyotypes, it is difficult to establish a relations...

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Detalles Bibliográficos
Autores principales: González-Rodríguez, María Teresa Alejandra, Brukman-Jiménez, Sinhue Alejandro, Cuero-Quezada, Idalid, Corona-Rivera, Jorge Román, Corona-Rivera, Alfredo, Serafín-Saucedo, Graciela, Aguirre-Salas, Liuba M., Bobadilla-Morales, Lucina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957150/
https://www.ncbi.nlm.nih.gov/pubmed/36833181
http://dx.doi.org/10.3390/genes14020253

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9957150/
https://www.ncbi.nlm.nih.gov/pubmed/36833181
http://dx.doi.org/10.3390/genes14020253

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