Ulnar mammary syndrome andTBX3: Expanding the phenotype
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33096/fullpdf
Reference19 articles.
1. Transcription factor Tbx3 is required for the specification of the atrioventricular conduction system;Bakker;Circ Res,2008
2. A gene for ulnar-mammary syndrome maps to 12q23-q24.1;Bamshad;Hum Mol Genet,1995
3. Mutations in hyman TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome;Bamshad;Nat Genet,1997
4. The spectrum of mutations in TBX3: Genotype/phenotype relationship in ulnar-mammary syndrome;Bamshad;Am J Hum Genet,1999
5. The levels of BMP4 signaling is critical fort he regulation of distinct T-box gene expression domains and growth along dorso-ventral axis of the optic cup;Behesti;BMC Dev Biol,2006
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