Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8166
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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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
- Schlagwort
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Erbkrankheit
Erbschaden
- Urheber
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Pavlistova, Lenka
- Beteiligte Personen und Organisationen
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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
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:31 MESZ
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Beteiligte
- Pavlistova, Lenka
- Izakova, Silvia
- Zemanova, Zuzana
- Bartuskova, Lucie
- Langova, Martina
- Malikova, Pavlina
- Michalová, Kyra
- SpringerLink (Online service)
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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
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TP53 abnormalities and chromosomal aneuploidy in acute panmyelosis with myelofibrosis
Chromosomal aberration arises during somatic reprogramming to pluripotent stem cells
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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
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