Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis

BACKGROUND: Constitutional translocations between sex chromosomes are rather rare in humans with breakpoints at Xp11 and Yq11 as the most frequent. Breakpoints on the short arm of the Y chromosome form one subgroup of t(X;Y), giving rise to a derived chromosome with the centromeres of both the X and...

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Detalles Bibliográficos
Autores principales: Pavlistova, Lenka, Izakova, Silvia, Zemanova, Zuzana, Bartuskova, Lucie, Langova, Martina, Malikova, Pavlina, Michalova, Kyra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007838/
https://www.ncbi.nlm.nih.gov/pubmed/27588041
http://dx.doi.org/10.1186/s13039-016-0276-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007838/
https://www.ncbi.nlm.nih.gov/pubmed/27588041
http://dx.doi.org/10.1186/s13039-016-0276-2

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