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Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 1, 1995
Identification, characterization, and localization to chromosome 17q21-22 of the human TBX2 homolog, member of a conserved developmental gene familyD J Law, T Gebuhr, N Garvey, et al.
Molecular Cell|February 13, 2001
A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexesS Bultman, T Gebuhr, D Yee, et al.
Nature Genetics|January 1, 1997
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyQ Y Li, R A Newbury-Ecob, J A Terrett, et al.
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