Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice

Author:

Ye Maoqing,Coldren Chris,Liang Xingqun,Mattina Teresa,Goldmuntz Elizabeth,Benson D. Woodrow,Ivy Dunbar,Perryman M.B.,Garrett-Sinha Lee Ann,Grossfeld Paul

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference38 articles.

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2. Clinical and molecular characterization of patients with distal 11q deletions;Penny;Am. J. Hum. Genet.,1995

3. Localization of Jacobsen syndrome breakpoints on a 40Mb. physical map of distal chromosome 11q;Tunnacliffe;Genome Res.,1999

4. The 11q terminal deletion disorder: a prospective study of 110 cases;Grossfeld;Am. J. Med. Genet.,2004

5. Molecular biology of the Ets family of transcription factors;Oikawa;Gene,2003

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