Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development

Erstveröffentlichung

2009

Authors

Zhang, Litu

Tumer, Zeynep

Mollgard, Kjeld

Barbi, Gotthold

Rossier, Eva

et al.

Wissenschaftlicher Artikel

Published in

European Journal of Human Genetics ; 17 (2009), 8. - S. 1010-1018. - ISSN 1018-4813. - eISSN 1476-5438

Link to publication

https://dx.doi.org/10.1038/ejhg.2008.269

Institutions

UKU. Institut für Humangenetik

Subject headings

[Free subject headings]: RUNX1T1 | MTG8 | ETO | acute myeloid leukemia (AML) | brain development | heart development | ACUTE MYELOID-LEUKEMIA | INTERVENTRICULAR SEPTUM | INTERSTITIAL DELETION | GENE | EXPRESSION | IDENTIFICATION | BREAKPOINTS | REGION
[DDC subject group]: DDC 570 / Life sciences

Metadata

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