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A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene
Muru, K., Kalev, I., Teek, R., Sõnajalg, M., Kuuse, K., Reimand, T., Õunap, K.Volume:
1
Year:
2010
Language:
english
Journal:
Molecular Syndromology
DOI:
10.1159/000330109
File:
PDF, 256 KB
english, 2010