10.1289/ehp.118-a353a - PMC

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The following terms were not found in PMC: 10.1289, ehp.118, ehp.118-a353a.
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Results: 2

Select item 17357271.

Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients

A Rauch, K Devriendt, A Koch, R Rauch, M Gewillig, C Kraus, M Weyand, H Singer, A Reis, M Hofbeck

J Med Genet. 2004 April; 41(4): e40. doi: 10.1136/jmg.2003.010975

PMCID:: PMC1735727

Summary PDF–417K

Select item 27748392.

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

Erich Roessler, Wuhong Pei, Maia V. Ouspenskaia, Jayaprakash D. Karkera, Jorge Ivan Veléz, Sharmilla Banerjee-Basu, Gretchen Gibney, Philip J. Lupo, Laura E. Mitchell, Jeffrey A. Towbin, Peter Bowers, John W. Belmont, Elizabeth Goldmuntz, Andreas D. Baxevanis, Benjamin Feldman, Maximilian Muenke

Mol Genet Metab. Author manuscript; available in PMC 2010 September 1.

Published in final edited form as: Mol Genet Metab. 2009 Sep–Oct; 98(1-2): 225–234. Published online 2009 May 27. doi: 10.1016/j.ymgme.2009.05.005