Nalaganje...
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...
Shranjeno v:
| izdano v: | Mol Cytogenet |
|---|---|
| Main Authors: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2016
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5007838/ https://ncbi.nlm.nih.gov/pubmed/27588041 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-016-0276-2 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|