A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene

Publisher: Karger

E-ISSN: 1661-8777|1|6|307-310

ISSN: 1661-8769

Source: Molecular Syndromology, Vol.1, Iss.6, 2011-08, pp. : 307-310

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Abstract