Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8166
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis ; volume:9 ; number:1 ; day:31 ; month:8 ; year:2016 ; pages:1-6 ; date:12.2016
Molecular cytogenetics ; 9, Heft 1 (31.8.2016), 1-6, 12.2016
- Keyword
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Erbkrankheit
Erbschaden
- Creator
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Pavlistova, Lenka
- Contributor
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Izakova, Silvia
Zemanova, Zuzana
Bartuskova, Lucie
Langova, Martina
Malikova, Pavlina
Michalová, Kyra
SpringerLink (Online service)
- DOI
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10.1186/s13039-016-0276-2
- URN
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urn:nbn:de:1111-201704175565
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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30.08.2024, 3:31 PM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Pavlistova, Lenka
- Izakova, Silvia
- Zemanova, Zuzana
- Bartuskova, Lucie
- Langova, Martina
- Malikova, Pavlina
- Michalová, Kyra
- SpringerLink (Online service)
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Prenatal diagnosis of ring chromosome 13: a rare chromosomal aberration
Chromosomal aberration arises during somatic reprogramming to pluripotent stem cells
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HMGA2 overexpression with specific chromosomal abnormalities predominate in CALR and ASXL1 mutated myelofibrosis
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Biological dosimetry: chromosomal aberration analysis for dose assessment
Primary immunodeficiency associated with chromosomal aberration – an ESID survey
TP53 abnormalities and chromosomal aneuploidy in acute panmyelosis with myelofibrosis
Prenatal diagnosis of ring chromosome 13: a rare chromosomal aberration
Chromosomal aberration arises during somatic reprogramming to pluripotent stem cells
Myelofibrosis
MYC chromosomal aberration in differential diagnosis between Burkitt and other aggressive lymphomas
HMGA2 overexpression with specific chromosomal abnormalities predominate in CALR and ASXL1 mutated myelofibrosis
Spherical aberration
Sphärische Aberration
Chromatische Aberration