T-box genes and congenital heart/limb malformations
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00314.x/fullpdf
Reference90 articles.
1. T-box genes in development: from hydra to humans;Papaioannou;Int Rev Cytol,2001
2. T-box genes and the formation of vertebrate forelimb- and hindlimb specific pattern;Simon;Cell Tissue Res,1999
3. Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype;Brassington;Am J Hum Genet,2003
4. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome;Merscher;Cell,2001
5. Newly identified paralogous groups on mouse chromosomes 5 and 11 reveal the age of a T-box cluster duplication;Ruvinsky;Genomics,1997
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1. TBX5 variant with the novel phenotype of mixed‑type total anomalous pulmonary venous return in Holt‑Oram Syndrome and variable intrafamilial heart defects;Molecular Medicine Reports;2022-05-04
2. TBX5;Current Topics in Developmental Biology;2017
3. Putative Breast Cancer Driver Mutations in TBX3 Cause Impaired Transcriptional Repression;Frontiers in Oncology;2015-10-29
4. The orthologous Tbx transcription factors Omb and TBX2 induce epithelial cell migration and extrusion in vivo without involvement of matrix metalloproteinases;Oncotarget;2014-09-02
5. Reconstruction and in vivo analysis of the extinct tbx5 gene from ancient wingless moa (Aves: Dinornithiformes);BMC Evolutionary Biology;2014-05-14
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