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A novel de novoTBX5mutation in a patient with Holt-Oram syn..:
Dreßen, Martina
;
Lahm, Harald
;
Lahm, Armin
...
Molecular Genetics & Genomic Medicine. 4 (2016) 5 - p. 557-567 , 2016
Link:
https://doi.org/10.1002/mgg3.234
RT Journal T1 <Title>A novel de novoTBX5mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_mgg3.234&Exemplar=1&LAN=DE A1 Dreßen, Martina A1 Lahm, Harald A1 Lahm, Armin A1 Wolf, Klaudia A1 Doppler, Stefanie A1 Deutsch, Marcus-André A1 Cleuziou, Julie A1 Pabst von Ohain, Jelena A1 Schön, Patric A1 Ewert, Peter A1 Malcic, Ivan A1 Lange, Rüdiger A1 Krane, Markus PB Wiley YR 2016 SN 2324-9269 JF Molecular Genetics & Genomic Medicine VO 4 IS 5 SP 557 OP 567 LK http://dx.doi.org/https://doi.org/10.1002/mgg3.234 DO https://doi.org/10.1002/mgg3.234 SF ELIB - SuUB Bremen
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